late pathophysiology difficult treatment endocrinology peds differential 21ohd classification

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21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase

, vomiting • Late ... #21HydroxylaseDeficiency #21OHD ... #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics

Lymphomas and Lymphoproliferative Disorders - Differential Diagnosis Algorithm
Hodgkin Lymphoma ~40% - Characteristic For Reed-Sternberg (RS) Cells

Lymphoproliferative Disorders - Differential ... Responsive to Treatment ... very high mitotic rate ... Lymphoproliferative #Disorders #Classification ... #pathophysiology

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