3 results
pathophysiology 21hydroxylasedeficiency endocrinology extremity leg lower newborn physicalexam praderwilli syndrome tone traction
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Prader-Willi Syndrome Signs ... fractures • Short ... PraderWilli #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
Pathogenesis and Clinical ... Signs/Symptoms/Complications ... pathophysiology #genetics ... endocrinology #peds ... #pediatrics
Tone - Leg Traction on Physical Exam Leg traction is done by holding the leg by the
until the buttock starts ... on the leg is a sign ... #PhysicalExam #clinical ... #video #peds #pediatrics
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