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21hydroxylasedeficiency 21ohd atlas beaus clinical diagnosis diseases endocrinology fingernails mees nail pathology pediatrics physicalexam terrys
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
• This is also ... Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
Nail Pathologies - Findings in or Near Nails Paronychia A superficial infection of the proximal and lateral
in innervation, genetics ... May arise from decreased ... psoriasis but also ... Nail #Diseases #Abnormal ... Diagnosis #Clinical #Signs
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