112 results
Prader-Willi Syndrome: Pathogenesis and clinical findings
 • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Prader-Willi Syndrome ... =>Prader-Willi Syndrome ... Signs/Symptoms ... delayed puberty -> Infertility ... #genetics #pathophysiology
Diabetes Insipidus vs Syndrome of Inappropriate ADH (SIADH) - Comparison Table

Diabetes Insipidus - Inadequate ADH
SIADH -
Diabetes Insipidus vs Syndrome ... Comparison #Table #Pathophysiology ... #Signs #Symptoms ... #Diagnosis #Endocrinology
Carcinoid Syndrome - Pathophysiology, Signs and Symptoms
Symptoms: Flushing, diarrhea, palpitations, bronchospasm
Complications: Carcinoid heart, mesenteric fibrosis, pellagra,
Carcinoid Syndrome ... - Pathophysiology ... #Carcinoid #Syndrome ... #Pathophysiology ... #Diagnosis
Cushing Syndrome - Hypercortisolism Differential Diagnosis Algorithm

#Cushings #Syndrome #Differential #Diagnosis #Algorithm #disease #endocrinology #Hypercortisolism
Cushing Syndrome ... Algorithm #Cushings ... #Syndrome #Differential ... #Diagnosis #Algorithm ... #disease #endocrinology
Acute Pancreatitis - Pathophysiology

#Pancreatitis #Pathophysiology #diagnosis #symptoms #signs #algorithm
Pancreatitis - Pathophysiology ... #Pancreatitis #Pathophysiology ... #diagnosis #symptoms ... #signs #algorithm
Adrenal Insufficiency - Differential Diagnosis Workup Algorithm
Primary Adrenal Insufficiency:
 • Autoimmune primary adrenal insufficiency
 • Adrenoleukodystrophy,
- Differential Diagnosis ... Workup Algorithm ... Adrenoleukodystrophy, genetic ... #Workup #Algorithm ... #endocrinology
Hypopituitarism Differential Diagnosis Algorithm
Suspected hypopituitarism (anterior pituitary)
Symptoms: fatigue, depression, and other endocrine dysfunction

ARUPConsult @ARUPLabs

#Hypopituitarism #Differential #Diagnosis
Algorithm Suspected ... anterior pituitary) Symptoms ... #Differential #Diagnosis ... #Algorithm #Pituitary ... #endocrinology
Infographic depicting the main pearls of various types of congenital adrenal hyperplasia for the medical student.
#CAH #algorithm ... CongenitalAdrenalHyperplasia #diagnosis ... treatment #Peds #Endocrinology ... #Adrenal #pathophysiology
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Signs/Symptoms/Complications ... Hirsutism & acne • Infertility ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology
A schema of the pathophysiology of the inborn errors of metabolism, excluding complex storage diseases. Helps
schema of the pathophysiology ... connections and pathophysiology ... MetabolicEmergency #Genetics ... #Pathophysiology ... #Diagnosis #Algorithm