3 results
pediatrics 21hydroxylasedeficiency 21ohd derm egd endocrinology gi metastatic praderwilli syndrome
Upper endoscopy revealed a pigmented mass in the duodenal bulb (Panel A) and two additional masses
portions of the duodenum ... (Panel B) #Clinical ... #GI #Derm #Honc ... #Melanoma #Duodenum ... EGD #Metastatic #NEJM
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Pathogenesis and clinical ... delayed puberty -> Infertility ... PraderWilli #Syndrome #genetics ... #pathophysiology ... #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 ... Hirsutism & acne • Infertility ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
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