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pediatrics genetics 21ohd cardiology congenital endocrinology fontan immune induced praderwilli procedure schematic syndrome thrombocytopenia thrombotic vaccine vitt
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Syndrome Signs/Symptoms ... Complications: • Gonadal hypoplasia ... Syndrome #genetics #pathophysiology ... #peds #pediatrics
Vaccine-induced immune thrombotic thrombocytopenia (VITT) is a rare but potentially serious adverse reaction that has been
vaccination with certain COVID ... Symptoms of VITT ... and neurological symptoms ... that while the diagram ... #pathophysiology
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Signs/Symptoms/Complications ... a scrotum #21HydroxylaseDeficiency ... #21OHD #pathophysiology ... endocrinology #peds
Fontan Procedure Schematic A Fontan is done in most children (approximately 90%) who effectively have a single
secondary to a hypoplastic ... Procedure #Schematic #Diagram ... congenital #Cardiology #Peds ... #Pediatrics #Pathophysiology
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