6 results
pediatrics radiology 21hydroxylasedeficiency 21ohd ct cxr derm diagnosis duodenum endocrinology gastriccancer henochscholeinpurpura hsp iga melanoma menetrier metastatic pediatricmenetrier praderwilli rugalhypertrophy
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
Upper endoscopy revealed a pigmented mass in the duodenal bulb (Panel A) and two additional masses
duodenum (Panel B) #Clinical ... #GI #Derm #Honc ... Melanoma #Duodenum #EGD ... #Metastatic #NEJM
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
Gastric Cancer in Chest Radiograph - A plain radiograph of the chest showed a round, irregular
#Clinical #Radiology ... #GI #Honc #CXR ... #EGD #GastricCancer ... #NEJM
Gastric Gyri - Pediatric Ménétrier’s Disease - Computed tomography with contrast material (Panel A shows the
#Clinical #Peds ... #GI #Radiology # ... CT #EGD #Menetrier ... RugalHypertrophy #NEJM
IgA Vasculitis – Henoch Scholein Purpura: Pathogenesis and Clinical Findings - Infectious Agents - 50% have
Pathogenesis and Clinical ... predisposition - Various genetic ... galactose-deficient IgA1 (GD-IgA1 ... nausea, vomiting, GI ... HenochScholeinPurpura #Pathophysiology
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