Primary hypogonadism, partial alopecia, and Müllerian hypoplasia: report of a fifth family and review

Primary hypogonadism combined with Müllerian hypoplasia and partial alopecia are common features of this syndrome, which was reported only in four earlier families from areas where consanguineous marriage is prevalent. An autosomal recessive pattern of inheritance was suggested earlier and is suppor...

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Detalles Bibliográficos
Autores principales: Al‐Obaidi, Ruqayah G. Y., Al‐Musawi, Bassam M. S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5628201/
https://www.ncbi.nlm.nih.gov/pubmed/29026561
http://dx.doi.org/10.1002/ccr3.1128
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author Al‐Obaidi, Ruqayah G. Y.
Al‐Musawi, Bassam M. S.
author_facet Al‐Obaidi, Ruqayah G. Y.
Al‐Musawi, Bassam M. S.
author_sort Al‐Obaidi, Ruqayah G. Y.
collection PubMed
description Primary hypogonadism combined with Müllerian hypoplasia and partial alopecia are common features of this syndrome, which was reported only in four earlier families from areas where consanguineous marriage is prevalent. An autosomal recessive pattern of inheritance was suggested earlier and is supported by this report.
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spelling pubmed-56282012017-10-12 Primary hypogonadism, partial alopecia, and Müllerian hypoplasia: report of a fifth family and review Al‐Obaidi, Ruqayah G. Y. Al‐Musawi, Bassam M. S. Clin Case Rep Case Reports Primary hypogonadism combined with Müllerian hypoplasia and partial alopecia are common features of this syndrome, which was reported only in four earlier families from areas where consanguineous marriage is prevalent. An autosomal recessive pattern of inheritance was suggested earlier and is supported by this report. John Wiley and Sons Inc. 2017-08-24 /pmc/articles/PMC5628201/ /pubmed/29026561 http://dx.doi.org/10.1002/ccr3.1128 Text en © 2017 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Reports
Al‐Obaidi, Ruqayah G. Y.
Al‐Musawi, Bassam M. S.
Primary hypogonadism, partial alopecia, and Müllerian hypoplasia: report of a fifth family and review
title Primary hypogonadism, partial alopecia, and Müllerian hypoplasia: report of a fifth family and review
title_full Primary hypogonadism, partial alopecia, and Müllerian hypoplasia: report of a fifth family and review
title_fullStr Primary hypogonadism, partial alopecia, and Müllerian hypoplasia: report of a fifth family and review
title_full_unstemmed Primary hypogonadism, partial alopecia, and Müllerian hypoplasia: report of a fifth family and review
title_short Primary hypogonadism, partial alopecia, and Müllerian hypoplasia: report of a fifth family and review
title_sort primary hypogonadism, partial alopecia, and müllerian hypoplasia: report of a fifth family and review
topic Case Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5628201/
https://www.ncbi.nlm.nih.gov/pubmed/29026561
http://dx.doi.org/10.1002/ccr3.1128
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