Endocrinology

Browse 97 topics in endocrinology.

97 results

Acromegaly

The condition is insidious, with a median delay in diagnosis of 7–10 years . During this period, patients develop significant comorbidities, including hypertension, diabetes mellitus, cardiomyopathy, and obstructive...

Pituitary Disorders4 Jan 2026Peer reviewed
Endocrinology
Neurosurgery
High evidence
+1

Acute Adrenal Crisis

An Acute Adrenal Crisis (Addisonian Crisis) is a life-threatening endocrine emergency resulting from an absolute or rela... MRCP exam preparation.

Acute Medicine6 Jan 2026Peer reviewed
Endocrinology
High evidence
MRCP

Acute Intermittent Porphyria (AIP)

AIP is often referred to as a "little imitator" because its symptoms—severe abdominal pain, psychiatric disturbances, and neurological deficits—mimic many common conditions, frequently leading to delayed diagnosis or...

Metabolic Medicine4 Jan 2026Peer reviewed
Endocrinology
Neurology
High evidence
+1

Addison's Disease (Primary Adrenal Insufficiency)

Addison's disease is primary adrenal insufficiency (PAI) caused by destruction or dysfunction of the adrenal cortex, res... MRCP exam preparation.

Adrenal9 Jan 2025Peer reviewed
Endocrinology
Emergency Medicine
High evidence
MRCP
+1
Emergency

Addisonian Crisis (Acute Adrenal Insufficiency)

Adrenal crisis presents with hypotension, hyponatraemia, hyperkalaemia, hypoglycaemia, and often hyperpigmentation (in p... ACEM Primary Written, ACEM Primary V

Other24 Jan 2026
Emergency Medicine
Endocrinology
High evidence
ACEM Primary Written

Adrenal Crisis

Adrenal crisis is an acute, life-threatening state of cortisol deficiency that requires immediate recognition and treatm... CICM Second Part exam preparation.

Peer reviewed
Intensive Care
Endocrinology
CICM Second Part
+3

Anorexia Nervosa (Adult)

Anorexia nervosa (AN) is a severe psychiatric disorder characterized by persistent restriction of energy intake leading to significantly low body weight (BMI less than 17.5 kg/m² in adults), an intense fear of gaining...

Eating Disorders7 Jan 2026Peer reviewed
Psychiatry
General Practice
+1

Autoimmune Polyglandular Syndrome (APS)

Autoimmune Polyglandular Syndromes (APS), also referred to as Autoimmune Polyendocrine Syndromes (APS) or Polyglandular ... MRCP exam preparation.

Autoimmune Endocrinology10 Jan 2026Peer reviewed
Endocrinology
Immunology
MRCP
+1

Calcium Disorders: Hypocalcemia and Hypercalcemia

Calcium gluconate 10% 10-20 mL IV over 10-20 minutes (0.9-1.8 mmol Ca2+)... CICM Second Part Written, CICM Second Part Hot Case exam preparation.

Electrolyte/Metabolic25 Jan 2026
Intensive Care Medicine
Nephrology
Moderate evidence
CICM Second Part Written
+1

Carcinoid Syndrome

Key Facts Tumour Origin : Midgut NETs (Appendix, Ileum) most common to cause syndrome. Syndrome Appears : Usually only after Liver Metastases (Hepatic first-pass metabolism bypassed). 10% of NET patients develop the...

Neuroendocrine Tumours10 Jan 2026Peer reviewed
Endocrinology
Oncology
High evidence
+1

Carcinoid Syndrome and Neuroendocrine Tumours

Neuroendocrine tumours (NETs) represent a heterogeneous group of neoplasms arising from neuroendocrine cells distributed... MRCP exam preparation.

Neuroendocrine Tumours5 Jan 2026Peer reviewed
Oncology
Gastroenterology
High evidence
MRCP
+1

Charcot Neuroarthropathy

The hallmark of acute Charcot is a red, hot, swollen foot in a patient with peripheral neuropathy, often triggered by minor trauma that goes unnoticed due to sensory loss. This acute inflammatory phase is...

Foot & Ankle6 Jan 2026Peer reviewed
Orthopaedics
Endocrinology
High evidence
+1

Congenital Adrenal Hyperplasia (CAH)

21-Hydroxylase Deficiency (21-OHD) accounts for 95% of all CAH cases and is the most common cause of: Ambiguous genitalia in genetic females (46,XX) Life-threatening salt-wasting crisis in neonates Primary adrenal...

Adrenal Disease6 Jan 2025Peer reviewed
Paediatrics
Endocrinology
High evidence

Conn's Syndrome (Primary Hyperaldosteronism)

Primary Hyperaldosteronism (PA) is the autonomous hypersecretion of aldosterone from the adrenal cortex (zona glomerulosa), leading to suppression of renin. It represents the most common cause of secondary...

Adrenal6 Jan 2026Peer reviewed
Endocrinology
General Practice
High evidence
+1

Conn's Syndrome (Primary Hyperaldosteronism)

Conn's syndrome, or primary aldosteronism (PA), represents the most common cause of secondary hypertension and potentially curable form of hypertension. First described by Jerome Conn in 1955, it is characterised by...

Adrenal9 Jan 2026Peer reviewed
Endocrinology
General Practice
High evidence
+2

Cushing's Syndrome

The most common cause worldwide is iatrogenic (exogenous glucocorticoid therapy), seen in patients receiving chronic corticosteroid treatment for inflammatory, autoimmune, or malignant conditions. Endogenous Cushing's...

Pituitary-Adrenal Axis6 Jan 2026Peer reviewed
Endocrinology
High evidence

Cushing's Syndrome

The pathophysiology involves systemic dysregulation of protein and fat metabolism, creating a catabolic state characterized by proximal muscle wasting, skin thinning, and paradoxical central obesity. Diagnostic...

Pituitary Surgery6 Jan 2026Peer reviewed
Endocrinology
Neurosurgery
High evidence
+1

Diabetes Insipidus (DI)

In health, AVP is synthesised in the hypothalamus and released from the posterior pituitary in response to rising plasma osmolality or falling blood volume, promoting water reabsorption in the renal collecting ducts...

Pituitary Disorders7 Jan 2026Peer reviewed
Endocrinology
Nephrology
High evidence
+1

Diabetic Foot Ulcer

A Diabetic Foot Ulcer (DFU) is a full-thickness wound below the ankle in a patient with diabetes mellitus, arising from the complex interaction of peripheral neuropathy, peripheral arterial disease, and biomechanical...

Podiatry6 Jan 2026Peer reviewed
Vascular Surgery
Endocrinology
High evidence
+1

Diabetic Ketoacidosis (Adult)

Diabetic Ketoacidosis (DKA) is a life-threatening acute metabolic emergency characterized by the pathognomonic triad of hyperglycemia , ketosis , and metabolic acidosis . It represents a state of absolute or relative...

Diabetes6 Jan 2026Peer reviewed
Endocrinology
Emergency Medicine
High evidence
+1

Diabetic Ketoacidosis (DKA)

Diabetic Ketoacidosis (DKA) is a profound metabolic emergency defined by the biochemical triad of Hyperglycaemia, Ketona... MRCP exam preparation.

Acute Medicine5 Jan 2026Peer reviewed
Endocrinology
High evidence
MRCP

Diabetic Nephropathy (Diabetic Kidney Disease)

Diabetic Nephropathy (DN), now comprehensively termed Diabetic Kidney Disease (DKD) , represents the leading cause of Chronic Kidney Disease (CKD) and End-Stage Renal Disease (ESRD) globally, accounting for...

Renal Medicine10 Jan 2026Peer reviewed
Nephrology
Endocrinology
High evidence
MRCP
+1

Diabetic Retinopathy

DR progresses through distinct stages: Non-Proliferative Diabetic Retinopathy (NPDR) – subdivided into Background (R1), Pre-Proliferative (R2) – and Proliferative Diabetic Retinopathy (PDR, R3) , characterised by...

Retina6 Jan 2026Peer reviewed
Ophthalmology
Endocrinology
High evidence
+1

Dyslipidaemia and Lipid Management

Dyslipidaemia encompasses a spectrum of lipid abnormalities characterized by elevated low-density lipoprotein cholestero... MRCP exam preparation.

Cardiovascular Prevention7 Jan 2026Peer reviewed
Cardiology
Endocrinology
MRCP
+2

Eating Disorders in Adults

Eating disorders are serious, potentially life-threatening mental health conditions characterised by persistent disturba... MRCPsych exam preparation.

Eating Disorders8 Jan 2026Peer reviewed
Psychiatry
General Practice
High evidence
MRCPsych
+1

Endocrine Physiology (Adrenal, Thyroid, Pituitary)

Endocrine physiology is fundamental to understanding the stress response in critical illness, metabolic regulation, and ... CICM First Part Written, CICM First

Endocrine Physiology25 Jan 2026
Intensive Care Medicine
Anaesthesia
CICM First Part Written
+1

Erectile Dysfunction

Erectile dysfunction (ED) is defined as the persistent or recurrent inability to achieve and/or maintain an erection suf... MRCS exam preparation.

Andrology9 Jan 2025Peer reviewed
Urology
Cardiology
High evidence
MRCS
+1

Fanconi Syndrome

The clinical hallmarks include: Renal glycosuria despite normoglycaemia Generalised aminoaciduria Phosphaturia leading to hypophosphataemic rickets/osteomalacia Type 2 (proximal) renal tubular acidosis from...

Tubular Disorders7 Jan 2026Peer reviewed
Nephrology
Endocrinology
High evidence
+1

Gastroparesis

The cardinal symptoms are nausea ( 90%), vomiting (particularly of undigested food hours after eating), early satiety , postprandial fullness , bloating , and abdominal pain . These symptoms are often debilitating and...

Motility Disorders7 Jan 2026Peer reviewed
Gastroenterology
Endocrinology

Gender Dysphoria (Gender Incongruence)

Gender Dysphoria is the clinical distress caused by a discrepancy between a person's Gender Identity (internally experienced gender) and their Sex Assigned at Birth . The condition is characterized by marked...

Gender Identity6 Jan 2026Peer reviewed
Psychiatry
Endocrinology
High evidence
+1

Gestational Diabetes Mellitus (GDM)

GDM is distinct from pre-existing diabetes mellitus (Type 1 or Type 2) diagnosed before pregnancy. The condition typically resolves within hours to days of placental delivery, as the primary driver of insulin...

Maternal-Fetal Medicine9 Jan 2026Peer reviewed
Obstetrics & Gynaecology
Endocrinology
High evidence

Glucagonoma

Dermatosis – Necrolytic Migratory Erythema (NME) Diabetes Mellitus – usually mild to moderate Deep Vein Thrombosis – hypercoagulable state Depression – neuropsychiatric manifestations

Neuroendocrine Tumours6 Jan 2026Peer reviewed
Endocrinology
Dermatology
High evidence
+2

Graves' Disease

Diffuse thyroid hyperplasia (smooth, diffusely enlarged goitre) Graves' Ophthalmopathy (Thyroid Eye Disease) - present in 25-50% of patients Pretibial myxoedema (dermopathy) - rare, less than 5% of cases Thyroid...

Thyroid6 Jan 2026Peer reviewed
Endocrinology
High evidence

Gynaecomastia

Physiological gynaecomastia occurs at three life stages: Neonatal (transplacental maternal oestrogen exposure, resolves within weeks), Pubertal (transient oestrogen-androgen imbalance, affects 60% of boys aged 10-16...

Male Breast Disease7 Jan 2026Peer reviewed
Endocrinology
General Practice
High evidence
+1

Hashimoto's Thyroiditis

Comprehensive, evidence-based guide to Hashimoto's Thyroiditis covering molecular pathophysiology, autoantibody testing, Levothyroxine management, pregnancy considerations, and complications including thyroid lymphoma.

Thyroid6 Jan 2026Peer reviewed
Endocrinology
General Practice
High evidence
MRCP

Hirsutism

Key Facts Definition : Excessive terminal hair growth in androgen-sensitive areas in women, quantified by modified Ferriman-Gallwey score ≥8. Prevalence : 5-15% of women of reproductive age; varies significantly by...

Reproductive Endocrinology10 Jan 2026Peer reviewed
Endocrinology
Dermatology
High evidence
+1

Hormone Replacement Therapy (HRT) Protocols

Hormone Replacement Therapy (HRT), also termed Menopausal Hormone Therapy (MHT) , involves the administration of systemic Oestrogen (with or without Progestogen ) to replace declining ovarian hormones in...

Menopause6 Jan 2026Peer reviewed
Obstetrics & Gynaecology
General Practice
High evidence
+2

Hypercalcaemia (Emergency)

Hypercalcaemia is a common and potentially life-threatening electrolyte disturbance defined by a corrected serum calcium... MRCP exam preparation.

Acute Medicine5 Jan 2026Peer reviewed
Endocrinology
High evidence
MRCP

Hyperosmolar Hyperglycaemic State (HHS)

Unlike Diabetic Ketoacidosis (DKA), HHS develops insidiously over days to weeks, leading to a much more profound fluid deficit (often 10–22 litres). The mortality rate of HHS remains high (15–20%), significantly...

Diabetic Emergencies4 Jan 2026Peer reviewed
Endocrinology
Acute Medicine
High evidence
+1

Hyperosmolar Hyperglycaemic State (HHS)

HHS is characterised by a relative insulin deficiency that is sufficient to prevent lipolysis and ketogenesis but insufficient to facilitate glucose utilisation or suppress hepatic gluconeogenesis. This results in...

Metabolic Emergency10 Jan 2026Peer reviewed
Endocrinology
Acute Medicine
High evidence
+2
Emergency

Hyperosmolar Hyperglycaemic State (HHS)

Hyperosmolar Hyperglycaemic State (HHS, formerly HONK/HHNS) is the most lethal hyperglycaemic emergency with 15-20% mort... ACEM Fellowship Written, ACEM Fellow

Endocrine Emergencies24 Jan 2026
Emergency Medicine
Endocrinology
High evidence
ACEM Fellowship Written

Hyperparathyroidism (Adult)

Hyperparathyroidism encompasses a spectrum of disorders characterised by excessive parathyroid hormone (PTH) secretion, ... MRCP exam preparation.

Calcium Disorders6 Jan 2026Peer reviewed
Endocrinology
Endocrine Surgery
High evidence
MRCP
+1

Hyperthyroidism in Adults

Hyperthyroidism is a clinical syndrome characterized by the excessive synthesis and secretion of thyroid hormones (thyro... MRCP, USMLE exam preparation.

Thyroidology11 Jan 2026Peer reviewed
Endocrinology
General Practice
High evidence
MRCP
Emergency

Hypoglycaemia - Emergency Management

Hypoglycaemia is a medical emergency defined by the clinical triad of low blood glucose (below 4.0 mmol/L in ED context)... ACEM Primary Written, ACEM Primary V

Endocrine Emergencies24 Jan 2026
Emergency Medicine
Endocrinology
High evidence
ACEM Primary Written

Hypoglycaemia in Adults

Hypoglycaemia is defined as blood glucose below 4.0 mmol/L (72 mg/dL) and represents one of the most common acute complications of diabetes management. It occurs when glucose delivery or production fails to meet...

Diabetes6 Jan 2025Peer reviewed
Emergency Medicine
Endocrinology
+1

Hypokalaemia

Clinical manifestations include muscle weakness, cramps, constipation, polyuria, and cardiac effects ranging from palpitations to ventricular arrhythmias. ECG changes are pathognomonic: U waves, flattened T waves, ST...

Intensive Care7 Jan 2026Peer reviewed
Emergency Medicine
Cardiology
+2

Hypomagnesaemia

The most important clinical consequences include life-threatening ventricular arrhythmias (particularly Torsades de Pointes), neuromuscular irritability (tetany, seizures), and electrolyte disturbances that cannot be...

Electrolyte Disorders7 Jan 2025Peer reviewed
Endocrinology
Gastroenterology
High evidence
+1

Hypoparathyroidism (Adult)

Hypoparathyroidism is a rare endocrine disorder characterized by insufficient secretion of parathyroid hormone (PTH) from the parathyroid glands, resulting in hypocalcaemia and hyperphosphataemia . Unlike other...

Calcium Disorders6 Jan 2026Peer reviewed
Endocrinology
ENT
High evidence
+1

Hypophosphataemia

The most clinically significant scenario is refeeding syndrome , where malnourished or starved patients develop acute, life-threatening hypophosphataemia upon carbohydrate refeeding due to rapid intracellular...

Electrolyte Disorders6 Jan 2026Peer reviewed
Endocrinology
Critical Care
+2

Hypothyroidism in Adults

Hypothyroidism is a common clinical syndrome resulting from a deficiency of thyroid hormones, which leads to a generaliz... MRCP, USMLE exam preparation.

Thyroid Disorders10 Jan 2026Peer reviewed
Endocrinology
General Practice
High evidence
MRCP

Insulinoma

Over 90% of insulinomas are benign, solitary, and less than 2 cm in diameter . Approximately 5-10% are associated with Multiple Endocrine Neoplasia Type 1 (MEN1) , where they may be multiple. Malignancy occurs in...

Neuroendocrine Tumours6 Jan 2026Peer reviewed
Endocrinology
General Surgery
+1

Kallmann Syndrome

The condition affects approximately 1 in 8,000 males and 1 in 40,000 females , with a male predominance of 4-5:1. Males typically present with absent pubertal development , micropenis , cryptorchidism , and...

Hypogonadism11 Jan 2026Peer reviewed
Endocrinology
Reproductive Medicine
High evidence
+1

Klinefelter Syndrome

The syndrome results from non-disjunction during parental meiosis, leading to testicular dysgenesis and progressive loss of seminiferous tubule function. The pathognomonic triad comprises hypergonadotropic...

Hypogonadism7 Jan 2026Peer reviewed
Endocrinology
Paediatrics
+1

Male Hypogonadism

Classic presentation involves reduced libido, erectile dysfunction, fatigue, and regression of secondary sexual characteristics. However, the clinical picture is highly variable depending on the age of onset...

Andrology11 Jan 2026Peer reviewed
Endocrinology
Urology
High evidence
+1

MEN-1 Syndrome

A comprehensive guide to MEN-1 Syndrome, covering the '3 Ps' (Parathyroid, Pituitary, Pancreas), the genetics of the MEN1 gene, molecular mechanisms, screening protocols, and evidence-based management.

Multiple Endocrine Neoplasia5 Jan 2025Peer reviewed
Endocrinology
Genetics
High evidence

Menopause Management

A comprehensive guide to Menopause management, covering HRT prescribing algorithms (Uterus vs No Uterus), risks (VTE, Breast Cancer), and managing Premature Ovarian Insufficiency.

Reproductive Health6 Jan 2026Peer reviewed
Obstetrics & Gynaecology
General Practice
High evidence
+1

Metabolic Dysfunction-Associated Steatotic Liver Disease (MASLD)

The global prevalence of MASLD is estimated at 25-30% of the general adult population, with significantly higher rates i... MRCP exam preparation.

Metabolic Medicine6 Jan 2026Peer reviewed
Gastroenterology
Endocrinology
High evidence
MRCP
+1

Metabolic Dysfunction-Associated Steatotic Liver Disease (MASLD)

Metabolic Dysfunction-Associated Steatotic Liver Disease (MASLD), formerly known as Non-Alcoholic Fatty Liver Disease (N... MRCP exam preparation.

Fatty Liver Disease7 Jan 2026Peer reviewed
Gastroenterology
Endocrinology
High evidence
MRCP
+1

Metabolic Syndrome

The unifying pathophysiological mechanism is Insulin Resistance , predominantly driven by excessive visceral adipose tissue accumulation. This creates a vicious cycle: adipose tissue dysfunction leads to ectopic fat...

Obesity6 Jan 2025Peer reviewed
Endocrinology
General Practice
High evidence
+1

Multiple Endocrine Neoplasia Type 2 (MEN 2)

A comprehensive, evidence-based guide to Multiple Endocrine Neoplasia Type 2 syndromes (MEN 2A and 2B), focusing on RET proto-oncogene mutations, genotype-phenotype correlations, prophylactic thyroidectomy timing,...

Thyroid Surgery10 Jan 2026Peer reviewed
Endocrinology
Genetics
High evidence
+2

Myxoedema Coma

Key Facts The "Winter Peak" : Over 90% of cases occur during winter months due to cold-induced stress on minimal thermogenic reserves. The T4-T3 Block : In severe illness, the peripheral conversion of T4 to active T3...

Thyroid Disease4 Jan 2026Peer reviewed
Endocrinology
Critical Care
High evidence
+2
Emergency

Myxoedema Coma

Myxoedema coma (myxedema crisis) is the extreme decompensated state of hypothyroidism with mortality 20-60% despite inte... ACEM Primary Written, ACEM Primary V

Endocrine Emergencies24 Jan 2026
Emergency Medicine
Endocrinology
High evidence
ACEM Primary Written

Neonatal Hypoglycaemia

The operational threshold for intervention varies between international guidelines, but the British Association of Perinatal Medicine (BAPM 2017) defines the intervention threshold as less than 2.6 mmol/L (47 mg/dL)...

Neonatal Care6 Jan 2026Peer reviewed
Paediatrics
Neonatology
High evidence
+1

Non-Alcoholic Fatty Liver Disease (NAFLD / MASLD)

Non-Alcoholic Fatty Liver Disease (NAFLD), recently renamed Metabolic Dysfunction-Associated Steatotic Liver Disease (MA... MRCP Part 2 exam preparation.

Metabolic Liver Disease7 Jan 2026Peer reviewed
Gastroenterology
Endocrinology
High evidence
MRCP Part 2
+1

Obesity Management

Obesity is a chronic, relapsing, neurohormonal disease characterised by excessive adipose tissue accumulation (Body Mass Index ≥30 kg/m²) that poses significant health risks. It represents one of the greatest public...

Metabolic Medicine6 Jan 2025Peer reviewed
Endocrinology
Bariatric Surgery
+1

Osteomalacia (Adult Rickets)

Osteomalacia is a metabolic bone disease characterised by defective mineralisation of the osteoid matrix in adults, resulting in the accumulation of unmineralised or inadequately mineralised bone. The term derives...

Metabolic Bone Disease6 Jan 2025Peer reviewed
Endocrinology
Orthopaedics
High evidence
+1

Osteomalacia & Rickets

Osteomalacia and rickets represent a spectrum of metabolic bone disorders characterised by defective mineralisation of b... MRCP exam preparation.

Metabolic Bone Disease6 Jan 2025Peer reviewed
Endocrinology
Orthopaedics
High evidence
MRCP
+1

Paget's Disease of Bone

The disease typically affects individuals over 55 years of age and is frequently asymptomatic, discovered incidentally through elevated serum alkaline phosphatase (ALP) or characteristic radiological findings. When...

Metabolic Bone Disease6 Jan 2026Peer reviewed
Rheumatology
Orthopaedics
High evidence
+1

Paget's Disease of Bone

A comprehensive guide to Paget's Disease of Bone, covering pathophysiology, the 'Cotton Wool' skull appearance, isolated raised Alkaline Phosphatase, bisphosphonate therapy, and complications including osteosarcoma.

Metabolic Bone Disease5 Jan 2025Peer reviewed
Endocrinology
Rheumatology
High evidence
MRCP
+1

Perioperative Diabetes Management: Glycemic Control, Insulin Protocols, and Hypoglycemia Prevention

Diabetes mellitus affects 10-15% of surgical patients , with perioperative hyperglycemia associated with increased morbidity including surgical site infections, delayed wound healing, cardiovascular events, and...

3 Feb 2026
ANZCA Final
Perioperative Medicine
+2

Peripheral Neuropathy

The hallmark of successful management lies in accurate phenotyping : Is it Axonal or Demyelinating? (NCS/EMG distinguishes). Is it Symmetric or Asymmetric? (Systemic vs Local/Vasculitis). Is it Large Fiber or Small...

Neuromuscular Disease5 Jan 2026Peer reviewed
Neurology
General Practice
High evidence
+1

Phaeochromocytoma and Paraganglioma

Phaeochromocytoma is a rare catecholamine-secreting tumour arising from chromaffin cells of the adrenal medulla. When arising from extra-adrenal sympathetic ganglia (paraganglia), the tumour is termed paraganglioma....

Adrenal Tumours7 Jan 2026Peer reviewed
Endocrinology
General Surgery
High evidence

Phaeochromocytoma Crisis

The cornerstone of acute management is alpha-adrenergic blockade FIRST using phentolamine (IV) or phenoxybenzamine (oral), followed only then by beta-blockade to control tachycardia. Beta-blockers administered alone...

Adrenal Surgery8 Jan 2026Peer reviewed
Emergency Medicine
Endocrinology
High evidence
+2

Phosphate and Magnesium Disorders in the ICU

Identify and treat underlying cause (refeeding, DKA treatment, diuretics, alcoholism)... CICM Second Part Written, CICM Second Part Hot Case exam preparation

Renal25 Jan 2026
Intensive Care Medicine
Nephrology
Moderate evidence
CICM Second Part Written
+1

Polycystic Ovarian Syndrome (PCOS)

Polycystic Ovarian Syndrome (PCOS) is the most common endocrine disorder in women of reproductive age, affecting approxi... MRCOG exam preparation.

Reproductive Medicine6 Jan 2026Peer reviewed
Obstetrics & Gynaecology
Endocrinology
High evidence
MRCOG
+1

Polycystic Ovary Syndrome (PCOS)

PCOS is not simply an ovarian disorder but a systemic metabolic condition with far-reaching health implications. Women with PCOS face substantially elevated risks of type 2 diabetes mellitus (4-fold increase),...

Reproductive Medicine6 Jan 2026Peer reviewed
Obstetrics & Gynaecology
Endocrinology
High evidence

Prader-Willi Syndrome (PWS)

Prader-Willi Syndrome (PWS) is a complex multisystem genetic disorder caused by loss of expression of paternally inherit... MRCPCH, FRACP exam preparation.

Genetic Syndromes10 Jan 2026Peer reviewed
Paediatrics
Endocrinology
High evidence
MRCPCH
+1

Premature Ovarian Insufficiency (POI)

Premature Ovarian Insufficiency (POI), previously termed Premature Ovarian Failure (POF), is defined as the loss of norm... MRCOG, USMLE exam preparation.

Reproductive Endocrinology11 Jan 2026Peer reviewed
Obstetrics & Gynaecology
Endocrinology
High evidence
MRCOG
+2

Primary Hyperaldosteronism

First described by Jerome Conn in 1955 as a syndrome of hypertension, hypokalaemia, and adrenal adenoma, PA was initially considered rare. However, the introduction of the aldosterone-renin ratio (ARR) as a screening...

Adrenal Disorders7 Jan 2025Peer reviewed
Endocrinology
General Practice
+1

Primary Hyperaldosteronism (Conn's Syndrome)

Primary Hyperaldosteronism (PA), also known as Primary Aldosteronism or Conn Syndrome (when due to an adenoma), represen... MRCP exam preparation.

Adrenal Disorders7 Jan 2026Peer reviewed
Endocrinology
Nephrology
High evidence
MRCP
+1

Primary Hyperparathyroidism

The condition is usually caused by a solitary parathyroid adenoma (80-85% of cases), though multigland hyperplasia (10-15%) and double adenomas (2-5%) also occur. Parathyroid carcinoma is rare, accounting for less...

Calcium Disorders8 Jan 2026Peer reviewed
Endocrinology
General Practice
High evidence
+1

Prolactinoma (Adult)

A prolactinoma is a benign monoclonal adenoma arising from lactotroph cells of the anterior pituitary that autonomously ... MRCP exam preparation.

Pituitary Disorders6 Jan 2026Peer reviewed
Endocrinology
Neurosurgery
High evidence
MRCP
+1

Rickets

While nutritional rickets (vitamin D deficiency) accounts for the majority of cases globally, clinicians must recognize genetic and metabolic forms including hypophosphataemic rickets, vitamin D-dependent rickets, and...

Bone6 Jan 2026Peer reviewed
Paediatrics
Endocrinology
High evidence
+1

Rickets and Osteomalacia

The underlying aetiology is multifactorial but globally dominated by Vitamin D Deficiency (nutritional rickets/osteomalacia), which remains a significant public health problem despite being entirely preventable....

Metabolic Bone Disease6 Jan 2025Peer reviewed
Paediatrics
Endocrinology
High evidence
+1

SIADH (Syndrome of Inappropriate ADH) - Adult

The Syndrome of Inappropriate Antidiuretic Hormone secretion (SIADH) is the most common cause of euvolaemic hyponatraemi... MRCP exam preparation.

Electrolytes6 Jan 2026Peer reviewed
Endocrinology
General Practice
High evidence
MRCP
+1

Stress Response and Critical Illness

The stress response to critical illness is a coordinated neuroendocrine-metabolic-inflammatory cascade designed for short-term survival. The HPA axis releases cortisol (essential for vascular tone and...

Basic Sciences - Physiology25 Jan 2026
Intensive Care Medicine
Endocrinology
High evidence
CICM First Part Written SAQ
+1

Syndrome of Inappropriate ADH Secretion (SIADH)

The Syndrome of Inappropriate Antidiuretic Hormone Secretion (SIADH), also termed Syndrome of Inappropriate Antidiuresis... MRCP, USMLE exam preparation.

Pituitary10 Jan 2026Peer reviewed
Endocrinology
Nephrology
High evidence
MRCP

Thyroid Cancer

The vast majority ( 90%) of thyroid cancers are differentiated thyroid cancers (DTC) , comprising papillary and follicular subtypes, which originate from thyroid follicular epithelial cells and retain the ability to...

Head and Neck6 Jan 2026Peer reviewed
Endocrinology
General Surgery
High evidence
+1

Thyroid Nodule (Adult)

A thyroid nodule is a discrete lesion within the thyroid gland that is radiologically distinct from the surrounding thyr... MRCP, FRACP exam preparation.

Thyroid Disorders9 Jan 2026Peer reviewed
Endocrinology
MRCP, FRACP

Thyroid Nodules & Goitre

Thyroid nodules are discrete lesions within the thyroid gland that are palpably or radiologically distinct from surrounding thyroid parenchyma. They represent one of the most common endocrine disorders, with a...

Endocrine Surgery6 Jan 2026Peer reviewed
Endocrinology
General Surgery
High evidence
+1

Thyroid Storm

Thyroid storm (thyrotoxic crisis) is a rare but life-threatening endocrine emergency characterized by severe, decompensa... MRCP exam preparation.

Thyroid Disease5 Jan 2026Peer reviewed
Endocrinology
Critical Care
Moderate evidence
MRCP
+1

Turner Syndrome (Child)

Turner syndrome (TS) is a chromosomal disorder affecting phenotypic females, characterised by complete or partial absenc... MRCPCH exam preparation.

Genetic Disorders6 Jan 2025Peer reviewed
Paediatrics
Genetics
High evidence
MRCPCH
+1

Type 1 Diabetes Mellitus

Comprehensive evidence-based guide to Type 1 Diabetes diagnosis, insulin management, technology, and complications

Diabetes9 Jan 2026Peer reviewed
Endocrinology
General Practice
+1

Type 2 Diabetes Mellitus

Type 2 Diabetes Mellitus (T2DM) is a chronic, progressive cardiorenal-metabolic syndrome characterized by hyperglycemia ... MRCP exam preparation.

Metabolic Medicine8 Jan 2026Peer reviewed
Endocrinology
High evidence
MRCP

Type 2 Diabetes Mellitus (Adult)

Type 2 Diabetes Mellitus (T2DM) is a chronic progressive metabolic disorder characterized by chronic hyperglycemia resul... MRCP, USMLE exam preparation.

Metabolic Medicine9 Jan 2026Peer reviewed
Endocrinology
General Practice
High evidence
MRCP

VIPoma

A VIPoma is an exceptionally rare functional pancreatic neuroendocrine tumour (pNET) that secretes excessive amounts of Vasoactive Intestinal Peptide (VIP). This hormone hypersecretion drives massive fluid and...

Neuroendocrine Tumours17 Jan 2026Peer reviewed
Endocrinology
Gastroenterology
High evidence
+1

Zollinger-Ellison Syndrome

Key Features : Sporadic : 75–80% of cases. Usually solitary pancreatic or duodenal tumours, potentially curable with surgical resection. MEN1-Associated : 20–25% of cases. Multiple gastrinomas, often microadenomas,...

Neuroendocrine Tumours6 Jan 2026Peer reviewed
Gastroenterology
Endocrinology
High evidence
+1