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21hydroxylasedeficiency clinical fingernails genetics pathophysiology pediatrics peds ridges transverse
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... Signs/Symptoms/Complications ... non-arousable, decr urine ... #21HydroxylaseDeficiency #21OHD ... pathophysiology #genetics #endocrinology
Transverse lines of the fingernails. (A) Beau’s lines (arrows) of the thumbnail. (B) Mees’ lines (arrowheads)
the nails can be caused ... are a typical sign ... #BeausLines #Transverse ... Ridges #Clinical #PhysicalExam ... #Photo
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