2 results
21hydroxylasedeficiency arthritis diagnosis endocrinology genetics
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 ... #pathophysiology ... endocrinology #peds ... #pediatrics
Combination of Skin Findings and Arthritis in Pediatrics Patient - Differential Diagnosis Malar rash: • A
Patient - Differential ... migrans: • Target sign ... gabrieltalledop #dermatology ... diagnosis #peds ... #pediatrics
No results found for "Carpal signs pathophysiology pediatrics differential causes dermatology dementia skin 21ohd peds"
Try removing search terms or sorting by relevance
Or Upload an image for you and others searching for #Carpal #signs #pathophysiology #pediatrics #differential #causes #dermatology #dementia #skin #21ohd #peds