2 results
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Females may be labeled ... Signs/Symptoms/Complications ... #21OHD #pathophysiology ... endocrinology #peds ... #pediatrics
Plantar Reflex on Newborn Physical Exam 
The normal response to stroking the lateral aspect of the
extension of the great toe ... toes or “Babinski sign ... #Plantar #Pyramidal ... PhysicalExam #clinical #video ... #peds #pediatrics