2 results
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD ... #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
Tone - Leg Traction on Physical Exam
Leg traction is done by holding the leg by the
on the leg is a sign ... Leg #Traction #Lower ... Extremity #tone #Newborn ... PhysicalExam #clinical #video ... #peds #pediatrics