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 ... enzyme 21-OHase causes ... non-arousable, decr urine ... #pathophysiology ... endocrinology #peds
Transverse lines of the fingernails. (A) Beau’s lines (arrows) of the thumbnail. (B) Mees’ lines (arrowheads)
are a typical sign ... of acute toxicity ... #BeausLines #Transverse ... #PhysicalExam # ... Photo