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diagnosis peds algorithm differential physicalexam treatment 21hydroxylasedeficiency 21ohd adrenal childhood clinical comparison congenitaladrenalhyperplasia examination excess genetics gh growthhormone hirsutism hypothyroid
Infographic depicting the main pearls of various types of congenital adrenal hyperplasia for the medical student.
#CAH #algorithm ... #causes #pediatrics ... treatment #Peds #Endocrinology ... #Adrenal #pathophysiology
Hirsutism - Differential Diagnosis Defined as excessive dark, coarse, male-pattern hair growth Hirsutism causes in premenopausal women: •
growth Hirsutism causes ... • Non-classic CAH ... Rare: Cushing's Syndrome ... , Acromegaly • ... Differential #Diagnosis #endocrinology
Growth Hormone Excess - Pathogenesis and clinical findings • Acromegaly and gigantism share the same pathophysiology
share the same pathophysiology ... • Other rare causes ... Carpal Tunnel Syndrome ... signs #symptoms #endocrinology ... #pathophysiology
Acromegaly - Diagnosis and Management Summary - GrepMed Handbook Clinical Presentation: • Classic Acromegaly: frontal
, hair growth, skin ... tags, skin thickening ... Beckwith Wiedemann syndrome ... or refractory cases ... Diagnosis #Management #Endocrinology
Tall Stature - Differential Diagnosis Algorithm Normal Growth (BA=CA) • Familial Tall Stature • XYY Syndrome Obese BMI
Normal Growth (BA=CA ... Stature • XYY Syndrome ... Resistance • Acromegaly ... Diagnosis #Algorithm #endocrinology ... #causes
Short Stature - Differential Diagnosis Algorithm Normal Variant, Normal Puberty Onset (BA = CA) • Familial Short
Puberty Onset (BA = CA ... Puberty Onset (BA < CA ... • Turner Syndrome ... Diagnosis #Algorithm #endocrinology ... #causes #pediatrics
Childhood Immunization Schedule: Why we immunize • Diphtheria Toxin -> URT inflammation causes pseudomembrane with hardened
that persists as skin ... > Inflammation causes ... if symptomatic can ... Immunization #peds #pediatrics ... #pathophysiology
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... cold & mottled skin ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
Myoedema in Hypothyroidism on Physical Exam Hypothyroidism is a clinical syndrome resulting from the production, secretion or
is a clinical syndrome ... symptoms that can ... dry and scaly skin ... reflex hammer, caused ... video #neurology #endocrinology
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 Newborn Infant - Routine Examination Birthweight, gestational age and birthweight percentile are noted. General observation Of the baby's
Down syndrome is ... with pigmented skin ... intra-abdominal masses ... defects of the skin ... Examination #Peds #Pediatrics
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