10 results
Thyroid Goiter on Physical Exam

Mother and daughter both presenting with thyroid goiters caused by iodine deficiency.
caused by iodine ... #PhysicalExam #iodine ... #deficiency #endocrinology ... #clinical #video ... #neck #hypothyroidism
Thyroid Goiter on Physical Exam

Mother and daughter both presenting with thyroid goiters caused by iodine deficiency.
caused by iodine ... #PhysicalExam #iodine ... #deficiency #endocrinology ... #clinical #video ... #neck #hypothyroidism
Pemberton's Sign caused by a Retrosternal Thyroid Goiter

Elevating the arms causes the previously flat neck veins
Pemberton's Sign caused ... Retrosternal Thyroid Goiter ... previously flat neck ... PhysicalExam #clinical #video ... #vascular #neck
Endemic Thyroid Goiter on Physical Exam

Note the movement of the thyroid mass with swallowing.

Dr. Bruno Farnetano
Endemic Thyroid Goiter ... #PhysicalExam #iodine ... #deficiency #endocrinology ... #clinical #video ... #neck #hypothyroidism
Hyperthyroidism Overview

Clinical Manifestation of Hyperthyroidism:
 • Fatigue
 • Weight loss
 • Heat intolerance
 • Depression, nervousness
Hyperdefecation • Anterior neck ... Toxic diffuse goiter ... Toxicosis • Iodine ... hyperthyroidism #causes ... #differential #endocrinology
Laboratory Evaluation of Patients for Thyroid Disease 
Hyperthyroidism:
 • Graves disease - TSH low; free T4
high; in some cases ... Toxic multinodular goiter ... increased radioactive iodine ... Euthyroid sick syndrome ... differential #diagnosis #endocrinology
Childhood Immunization Schedule: Why we immunize
 • Diphtheria Toxin -> URT inflammation causes pseudomembrane with hardened
SOB, N/V, stiff neck ... onset of fever, neck ... • Varicella-Zoster ... Immunization #peds #pediatrics ... #pathophysiology
Brudzinski’s Sign in Meningitis (first described in 19th century by Dr. Josef Brudzinski)

Brudzinski's sign is characterized
Passive neck flexion ... causes spinal cord ... While the pathophysiology ... Video by Dr. ... #PhysicalExam #Pediatrics
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
mutation in CYP21A2 coding ... enzyme 21-OHase causes ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
Acromegaly - Diagnosis and Management Summary - GrepMed Handbook 

Clinical Presentation: 
 • Classic Acromegaly: frontal
macroglossia, goiter ... malignancy Pathophysiology ... Beckwith Wiedemann syndrome ... or refractory cases ... Diagnosis #Management #Endocrinology