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  • Title: [Congenital adrenal hyperplasia due to 21-hydroxylase deficiency].
    Author: Fujieda K, Mukai T.
    Journal: Nihon Rinsho; 2004 Feb; 62(2):361-7. PubMed ID: 14968546.
    Abstract:
    21-hydroxylase deficiency occurring in one of 15,000 live births represents the most frequent disorder in female pseudohermaphroditism. Molecular genetic analysis is useful for ascertaining disease condition. Newborn mass-screening has been conducted in Japan. Prenatal diagnosis and treatment is feasible.
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