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pathophysiology diagnosis signs 21hydroxylasedeficiency 21ohd achilles cirrhosis endocrinology hepatology liverfailure msk praderwilli syndrome tendonrupture
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
findings • Maternal ... Prader-Willi Syndrome Signs ... /Symptoms/Complications ... pathophysiology #peds ... #pediatrics
Achilles Tendon Rupture - Pathogenesis and clinical findings • The Achilles tendon is 15cm long in
Pathogenesis and clinical ... findings • The ... is 15cm long in adults ... Thompson calf squeeze test ... #msk #orthopedics
Clinical features of Liver Disease in Children #Cirrhosis #LiverFailure #Signs #Symptoms #PhysicalExam #Findings #Diagnosis #Peds #Pediatrics #Hepatology **
Clinical features ... #LiverFailure #Signs ... #Symptoms #PhysicalExam ... #Findings #Diagnosis ... #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 ... Findings Autosomal ... Signs/Symptoms/Complications ... endocrinology #peds ... #pediatrics
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