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Congenital adrenal hyperplasia owing to 17α-hydroxylase/17,20 lyase and p450 oxidoreductase deficiencies.

Advances in experimental medicine and biology - 1 Jan 2011

Flück Christa E

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Share to Adrenal Hyperplasia, Congenital
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Share to NADPH-Ferrihemoprotein Reductase
Share to Steroid 17-alpha-Hydroxylase

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PMID: 21691943
DOI: 10.1007/978-1-4419-8002-1_1

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Congenital adrenal hyperplasia owing to 17α-hydroxylase/17,20 lyase and p450 oxidoreductase deficiencies.PMID 21691943Read ↗

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Congenital adrenal hyperplasia and P450 oxidoreductase deficiency.Semantic proximity Read ↗

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A Rare Cause of Congenital Adrenal Hyperplasia: Clinical and Genetic Findings and Follow-up Characteristics of Six Patients with 17-Hydroxylase Deficiency Including Two Novel MutationsSemantic proximity Read ↗

The syndrome of 17,20 lyase deficiency.Semantic proximity Read ↗

Combined 17α-hydroxylase/17,20-lyase deficiency due to p.R96W mutation in the CYP17 gene in a Brazilian patient.Semantic proximity Read ↗

Clinical and genetic analyses of a Chinese female with 17α-hydroxylase/17,20-lyase deficiency.Semantic proximity Read ↗

Two rare forms of congenital adrenal hyperplasia, 11β hydroxylase deficiency and 17-hydroxylase/17,20-lyase deficiency, presenting with novel mutations.Semantic proximity Read ↗

Genetics of congenital adrenal hyperplasia.Semantic proximity Read ↗

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