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pediatrics genetics 21ohd cardiology congenital covid cryptogenic diagnosis endocrinology fontan immune induced management organizing pneumonia praderwilli procedure pulmonary schematic syndrome
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Loss of parental copy ... Syndrome Signs/Symptoms ... Complications: • Gonadal hypoplasia ... 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
Signs/Symptoms/Complications ... a scrotum #21HydroxylaseDeficiency ... #21OHD #pathophysiology ... endocrinology #peds
Vaccine-induced immune thrombotic thrombocytopenia (VITT) is a rare but potentially serious adverse reaction that has been
Symptoms of VITT ... and neurological symptoms ... that while the diagram ... ChAdOx1 or Ad26-CoV ... thrombocytopenia #COVID #pathophysiology
Cryptogenic Organizing Pneumonia - Illness Script PATHOPHYSIOLOGY: Unknown trigger, reversible inflammatory/fibroproliferative process. Polypoid fibroblastic aggregates that plug
Illness Script PATHOPHYSIOLOGY ... Females SIGNS/SYMPTOMS ... • Symptoms: Cough ... identified (autoimmune, meds ... TylerLarsenMD #COP
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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