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21hydroxylasedeficiency 21ohd clinical endocrinology pathophysiology pediatrics peds radiology sign throckmorton throckmortonsign xraypelvis
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... scrotum & enlarged penis ... may look like a penis ... pathophysiology #genetics
Positive Throckmorton sign in a case of chronic osteomyelitis of the left hip. X-ray findings: 1) complete
Throckmorton sign in a case ... refers to when the penis ... ThrockmortonSign #Enchondroma
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