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 ... enzyme 21-OHase causes ... pathophysiology #genetics ... endocrinology #peds ... #pediatrics
Tone - Hand Position on Physical Exam

A newborn baby’s hand is held in a fisted position
Physical Exam A newborn ... hand will often cause ... neuron lesion in an infant ... #PhysicalExam #clinical ... #video #peds #pediatrics
Newborn Infant - Routine Examination

Birthweight, gestational age and birthweight percentile are noted.
General observation Of the baby's
Newborn Infant - ... paediatrician or geneticist ... #Newborn #Infant ... #Examination #Peds ... #Pediatrics #Diagnosis