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diagnosis 21hydroxylasedeficiency arthritis disorders endocrinology genetics history pathophysiology primarycare
Combination of Skin Findings and Arthritis in Pediatrics Patient - Differential Diagnosis Malar rash: • A
Patient - Differential ... migrans: • Target sign ... gabrieltalledop #dermatology ... diagnosis #peds ... #pediatrics
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... Signs/Symptoms/Complications ... cold & mottled skin ... endocrinology #peds ... #pediatrics
Helpful Clinical Features in Evaluating Bleeding Disorders Age of onset • Neonate - in 20% of haemophilias,
Helpful Clinical ... and skin haemorrhage ... #History #peds ... #pediatrics #diagnosis ... #hematology #primarycare
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