Primary hypogonadism, partial alopecia, and Müllerian hypoplasia: report of a fifth family and review-Reference-Cited by-同舟云学术

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

Published:2017-08-24 Issue:10 Volume:5 Page:1634-1638
ISSN:2050-0904
Container-title:Clinical Case Reports
language:en
Short-container-title:Clin Case Rep

Author:

Al-Obaidi Ruqayah G. Y.¹,Al-Musawi Bassam M. S.²^ORCID

Affiliation:

1. Medical Genetics; Genetic Counseling Clinic & Laboratory; The Teaching Laboratories; Baghdad Medical City; Baghdad Iraq

2. Medical Genetics; College of Medicine; University of Baghdad; Baghdad Iraq

Publisher

Wiley

Subject

General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ccr3.1128/fullpdf

Reference11 articles.

1. A familial syndrome of deafness, alopecia, and hypogonadism;Crandall;J. Pediatr.,1973

2. Progressive extrapyramidal disorder with primary hypogonadism and alopecia in sibs: a new syndrome?;Devriendt;Am. J. Med. Genet.,1996

3. Alopecia-mental retardation syndrome associated with convulsions and hypergonadotropic hypogonadism;Devriendt;Clin. Genet.,1996

4. A newly recognized neuroectodermal syndrome of familial alopecia, anosmia, deafness, and hypogonadism;Johnson;Am. J. Med. Genet.,1983

5. Alopecia-anosmia deafness-hypogonadism syndrome revisited: report of a new case;Johnston;Am. J. Med. Genet.,1987

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