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