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diagnosis 21hydroxylasedeficiency 21ohd algorithm cah causes childhood comparison congenitaladrenalhyperplasia examination genetics henochschonleinpurpura hsp igav immunization infant insufficiency newborn nightmares parasomnias
Infographic depicting the main pearls of various types of congenital adrenal hyperplasia for the medical student.
of congenital adrenal ... algorithm #causes #pediatrics ... comparison #treatment #Peds ... #Endocrinology ... #Adrenal #pathophysiology
Primary vs Secondary Adrenal Insufficiency - Pathophysiology Primary AI = adrenal glands themselves are the problem. This
Insufficiency - Pathophysiology ... Primary AI = adrenal ... UCSD Internal Medicine ... Insufficiency #Pathophysiology ... #endocrinology
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
21-OHD in the adrenal ... cold & mottled skin ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
Diagnosis of IgA Vasculitis (Henoch-Schönlein Purpura) - French Vasculitis Study Group 1) Suggestive clinical manifestations
complications - Renal ... especially in the skin ... arterioles in the skin ... #Rheumatology #Peds ... #Pediatrics
Pediatric Parasomnias and Nightmares: Pathogenesis and clinical findings Parasomnias - Micro-arousal episodes during SWS -> Intense activation of
Pediatric Parasomnias ... Speech • Flushed skin ... Parasomnias #Nightmares #Pediatrics ... #Peds #pathophysiology
Childhood Immunization Schedule: Why we immunize • Diphtheria Toxin -> URT inflammation causes pseudomembrane with hardened
that persists as skin ... #Immunization #peds ... #pediatrics #pathophysiology
Newborn Infant - Routine Examination Birthweight, gestational age and birthweight percentile are noted. General observation Of the baby's
with pigmented skin ... which are usually renal ... defects of the skin ... #Examination #Peds ... #Pediatrics #Diagnosis
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