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genetics pediatrics 21hydroxylasedeficiency 21ohd cardiogenic cardiology diagnosis praderwilli syndrome
Cardiogenic Shock: Pathogenesis, complications and clinical findings #Cardiogenic #Shock #pathophysiology #cardiology #diagnosis #signs #symptoms
Cardiogenic Shock ... Pathogenesis, complications ... #pathophysiology ... #cardiology #diagnosis ... #signs #symptoms
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Prader-Willi Syndrome Signs ... /Symptoms/Complications ... , sleep apnea, cor ... 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 ... vomiting • Late (shock ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
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