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21hydroxylasedeficiency abnormal atlas clinical diagnosis diseases fingernails mees nail pathology pediatrics peds physicalexam signs terrys
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
, vomiting • Late ... #21HydroxylaseDeficiency #21OHD ... #pathophysiology ... #genetics #endocrinology
Nail Pathologies - Findings in or Near Nails Paronychia A superficial infection of the proximal and lateral
in innervation, genetics ... causes include diabetes ... failure, and diabetes ... Linear Depressions (Beau's ... PhysicalExam #Atlas #Beaus
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