A Case of 3β-Hydroxysteroid Dehydrogenase Type II (HSD3B2) Deficiency Picked up by Neonatal Screening for 21-Hydroxylase Deficiency: Difficulties and Delay in Etiologic Diagnosis

Publisher: Karger

E-ISSN: 1663-2826|68|4|204-208

ISSN: 1663-2818

Source: Hormone Research in Paediatrics, Vol.68, Iss.4, 2007-05, pp. : 204-208

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Abstract