Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12188/10995
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dc.contributor.authorMirjana Kocovaen_US
dc.contributor.authorVioleta Anastasovskaen_US
dc.contributor.authorIskra Bitovskaen_US
dc.date.accessioned2021-03-16T10:45:14Z-
dc.date.available2021-03-16T10:45:14Z-
dc.date.issued2019-06-19-
dc.identifier.urihttp://hdl.handle.net/20.500.12188/10995-
dc.description.abstractThe simple virilizing (SV) form of congenital adrenal hyperplasia (CAH) is an autosomal recessive disorder usually caused by steroid 21-hydroxylase deficiency due to I172N missense mutation at the CYP21A2 gene. Clinical presentation encompasses virilization of external genitalia in newborn females and pseudoprecocious puberty in both sexes, due to reactive androgen overproduction. The aim of this study was to present two sisters with an SV form of CAH and distinctive genotype, detected and treated since childhood with a poor compliance and poor metabolic control hindering the fertility.en_US
dc.language.isoenen_US
dc.publisherBMC Part of Springer Natureen_US
dc.relation.ispartofEuropean Journal of Medical Researchen_US
dc.titleThe impact of CYP21A2 (P30L/I172N) genotype on female fertility in one familyen_US
dc.typeArticleen_US
dc.identifier.doi10.1186/s40001-019-0379-4-
dc.identifier.urlhttp://link.springer.com/content/pdf/10.1186/s40001-019-0379-4.pdf-
dc.identifier.urlhttp://link.springer.com/article/10.1186/s40001-019-0379-4/fulltext.html-
dc.identifier.urlhttp://link.springer.com/content/pdf/10.1186/s40001-019-0379-4.pdf-
dc.identifier.volume24-
dc.identifier.issue1-
item.grantfulltextnone-
item.fulltextNo Fulltext-
crisitem.author.deptFaculty of Medicine-
crisitem.author.deptFaculty of Medicine-
Appears in Collections:Faculty of Medicine: Journal Articles
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