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21hydroxylasedeficiency bruising endocrinology facial genetics newborn pathophysiology
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
Facial bruising- Marked bruising of the face can occur during delivery. It is more common when
difficult, or when the infant ... When the infant ... the body, the diagnosis ... #peds #pediatrics ... #clinical #photo
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