A rare cause of congenital adrenal hyperplasia: Antley-Bixler syndrome due to POR deficiency.

Herkert, J C; Blaauwwiekel, E E; Hoek, A; Veenstra-Knol, H E; Kema, I P; Arlt, W; Kerstens, M N

Herkert, J C; Blaauwwiekel, E E; Hoek, A; Veenstra-Knol, H E; Kema, I P; Arlt, W; Kerstens, M N.

Affiliation

Herkert JC; Department of Genetics, University Medical Centre Groningen, University of Groningen, the Netherlands. j.c.herkert@medgen.umcg.nl

Neth J Med ; 69(6): 281-3, 2011 Jun.

Article in En | MEDLINE | ID: mdl-21868813

Subject(s)

Adrenal Hyperplasia, Congenital/genetics; Antley-Bixler Syndrome Phenotype/genetics; NADPH-Ferrihemoprotein Reductase/deficiency; Adrenal Hyperplasia, Congenital/diagnosis; Adrenal Hyperplasia, Congenital/etiology; Female; Humans; Menstruation Disturbances/etiology; Young Adult

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Collection: 01-internacional Database: MEDLINE Main subject: NADPH-Ferrihemoprotein Reductase / Adrenal Hyperplasia, Congenital / Antley-Bixler Syndrome Phenotype Type of study: Diagnostic_studies / Etiology_studies Limits: Adult / Female / Humans Language: En Journal: Neth J Med Year: 2011 Document type: Article Affiliation country: Netherlands Country of publication: Netherlands

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