Literature DB >> 4061495

Primary hypogonadism and partial alopecia in three sibs with müllerian hypoplasia in the affected females.

S A Al-Awadi, T I Farag, A S Teebi, K Naguib, M Y el-Khalifa, Y Kelani, A Al-Ansari, R N Schimke.   

Abstract

We describe 3 sibs, two females and a male, with hypogonadism, defective Müllerian development in the sisters, and partial alopecia consisting of cranial hair only in the center of the scalp. One sister had absent gonads, the other had streak ovaries; both had markedly hypoplastic internal genitalia. Their brother had hormonal and histologic findings consistent with germinal cell aplasia. In view of the fact that the parents were consanguineous, autosomal recessive inheritance of the syndrome is likely.

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Year:  1985        PMID: 4061495     DOI: 10.1002/ajmg.1320220322

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  8 in total

Review 1.  Endocrine disorders in Woodhouse-Sakati syndrome: a systematic review of the literature.

Authors:  M Agopiantz; P Corbonnois; A Sorlin; C Bonnet; M Klein; N Hubert; V Pascal-Vigneron; P Jonveaux; T Cuny; B Leheup; G Weryha
Journal:  J Endocrinol Invest       Date:  2014-01-08       Impact factor: 4.256

2.  Primary amenorrhoea secondary to two different syndromes: a case study.

Authors:  Zareen Kiran; Tayyaba Jamil
Journal:  BMJ Case Rep       Date:  2019-03-15

3.  Mayer-Rokitansky-Küster-Hauser Syndrome with Alopecia: A Rare Case Report with Review of Literature.

Authors:  Sanjiv V Choudhary; Uday V Choudhari
Journal:  Int J Trichology       Date:  2016 Jul-Sep

4.  Unusual association of Turner syndrome and Mayer-Rokitansky-Küster-Hauser syndrome.

Authors:  Alpana Meena; Mradul Kumar Daga; Rashmi Dixit
Journal:  BMJ Case Rep       Date:  2016-05-20

Review 5.  Autosomal recessive disorders among Arabs: an overview from Kuwait.

Authors:  A S Teebi
Journal:  J Med Genet       Date:  1994-03       Impact factor: 6.318

6.  Coexistence of gonadal dysgenesis and Mayer-Rokitansky-Kuster-Hauser syndrome in 46, XX female: A case report and review of literature.

Authors:  Viral N Shah; Parth J Ganatra; Rajni Parikh; Panna Kamdar; Seema Baxi; Nishit Shah
Journal:  Indian J Endocrinol Metab       Date:  2013-10

7.  Phenotypic Variability of c.436delC DCAF17 Gene Mutation in Woodhouse-Sakati Syndrome.

Authors:  Mohammad Almeqdadi; Jennifer L Kemppainen; Pavel N Pichurin; Ralitza H Gavrilova
Journal:  Am J Case Rep       Date:  2018-03-25

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

Authors:  Ruqayah G Y Al-Obaidi; Bassam M S Al-Musawi
Journal:  Clin Case Rep       Date:  2017-08-24
  8 in total

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