9 results
Thyroid Goiter on Physical Exam

Mother and daughter both presenting with thyroid goiters caused by iodine deficiency.
Thyroid Goiter on ... goiters caused ... by iodine deficiency ... #deficiency #endocrinology ... #clinical #video
Causes of Apparent Life Threatening Event (ALTE) - Differential Diagnosis Algorithm
Cardiac:
 • Congenital Heart Disease
 •
Causes of Apparent ... Differential Diagnosis Algorithm ... Gastroesophageal Reflux ... #Causes #Peds # ... Pediatrics
Myoedema in Hypothyroidism on Physical Exam

Hypothyroidism is a clinical syndrome resulting from the production, secretion or
inadequate action of thyroid ... receptors for thyroid ... abolished tendon reflexes ... hammer, caused ... video #neurology #endocrinology
Pediatric Vomiting - Gastrointestinal and Systemic Causes - Differential Diagnosis Algorithm
Hepatobiliary:
 • Acute Hepatitis
 • Acute
Pediatric Vomiting ... Gastroesophageal Reflux ... Addison's Disease • Thyroid ... #Causes #Peds # ... Pediatrics
Hyperthyroidism Overview

Clinical Manifestation of Hyperthyroidism:
 • Fatigue
 • Weight loss
 • Heat intolerance
 • Depression, nervousness
Hyperthyroidism Overview Clinical ... Toxicosis • Iodine ... Thionamide - Iodine ... hyperthyroidism #causes ... #differential #endocrinology
Approach to Thyroid Function Tests in the Evaluation of Hyperthyroidism
 • Low TSH, Low normal T4
Approach to Thyroid ... of pregnancy, critical ... → Radioactive Iodine ... Hyperthyroidism #algorithm ... #diagnosis #endocrinology
Thyroid Goiter on Physical Exam

Mother and daughter both presenting with thyroid goiters caused by iodine deficiency.
Thyroid Goiter on ... goiters caused ... by iodine deficiency ... #deficiency #endocrinology ... #clinical #video
Hypothyroidism - Differential Diagnosis Algorithm
Central Hypothyroidism
 • Isolated TSH Deficiency
 • Panhypopituitarism
Thyroid Hormone Resistance
Iatrogenic
Primary Hypothyroidism
 -
Differential Diagnosis Algorithm ... Panhypopituitarism Thyroid ... • Severe Iodine ... #endocrinology ... #causes
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... mutation in CYP21A2 coding ... enzyme 21-OHase causes ... pathophysiology #genetics #endocrinology ... #peds #pediatrics