3 results
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... deficiencies present in infants ... Signs/Symptoms/Complications ... endocrinology #peds ... #pediatrics
Primitive Suck, Rooting Reflex on Newborn Physical Exam 
The normal response to stroking the lateral aspect
Primitive Suck, ... toes or “Babinski sign ... normal in the infant ... #PhysicalExam #clinical ... #video #peds #pediatrics
Plantar Reflex on Newborn Physical Exam 
The normal response to stroking the lateral aspect of the
toes or “Babinski sign ... normal in the infant ... Plantar #Pyramidal #Primitive ... #PhysicalExam #clinical ... #video #peds #pediatrics