12 results
Thyroid Goiter on Physical Exam

Mother and daughter both presenting with thyroid goiters caused by iodine deficiency.
thyroid goiters caused ... by iodine deficiency ... #PhysicalExam #iodine ... #deficiency #endocrinology ... hypothyroidism #otolaryngology
Web chart of various etiologies related to congenital neck masses.

#differential #causes #pediatrics #congenital #neck #head #masses
congenital neck masses ... #differential #causes ... #pediatrics #congenital ... #neck #head #masses ... #otolaryngology
Differentiation of Causes of Hyperthyroidism According to Pattern of Radionucleotide Uptake
Reduced uptake:
 • Thyroiditis
 • Exogenous
Differentiation of Causes ... thyroxine • Iodine ... #radioactive #iodine ... radionuclide #uptake #differential ... hyperthyroidism #endocrinology
Web chart of etiologies related to neoplastic neck masses.

#pediatrics #differential #neoplastic #head #neck #masses #otolaryngology #ent
neoplastic neck masses ... #pediatrics #differential ... neoplastic #head #neck #masses ... #otolaryngology
Infographic depicting the main pearls of various types of congenital adrenal hyperplasia for the medical student.
CAH #algorithm #causes ... #pediatrics #CongenitalAdrenalHyperplasia ... treatment #Peds #Endocrinology ... #Adrenal #pathophysiology
Thyroid Goiter on Physical Exam

Mother and daughter both presenting with thyroid goiters caused by iodine deficiency.
thyroid goiters caused ... by iodine deficiency ... #PhysicalExam #iodine ... #deficiency #endocrinology ... hypothyroidism #otolaryngology
Hyperthyroidism Overview

Clinical Manifestation of Hyperthyroidism:
 • Fatigue
 • Weight loss
 • Heat intolerance
 • Depression, nervousness
Toxicosis • Iodine ... Thionamide - Iodine ... hyperthyroidism #causes ... #diagnosis #differential ... #endocrinology
Laboratory Evaluation of Patients for Thyroid Disease 
Hyperthyroidism:
 • Graves disease - TSH low; free T4
high; in some cases ... increased radioactive iodine ... increased radioactive iodine ... #hyperthyroid #differential ... #diagnosis #endocrinology
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
Short Stature - Differential Diagnosis Algorithm
Normal Variant, Normal Puberty Onset (BA = CA)
 • Familial Short
Short Stature - Differential ... #ShortStature #Differential ... Diagnosis #Algorithm #endocrinology ... #causes #pediatrics