Literature DB >> 4698933

A familial syndrome of deafness, alopecia, and hypogonadism.

B F Crandall, L Samec, R S Sparkes, S W Wright.   

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Year:  1973        PMID： 4698933     DOI： 10.1016/s0022-3476(73)80121-0

Source DB:  PubMed          Journal:  J Pediatr        ISSN： 0022-3476            Impact factor:   4.406


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  10 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.  Congenital universal alopecia, mental deficiency, and microcephaly in two sibs.

Authors:  R A Pfeiffer; J Völklein
Journal:  J Med Genet       Date:  1982-10       Impact factor: 6.318

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.  A syndrome of hypogonadism, alopecia, diabetes mellitus, mental retardation, deafness, and ECG abnormalities.

Authors:  N J Woodhouse; N A Sakati
Journal:  J Med Genet       Date:  1983-06       Impact factor: 6.318

5.  Bjornstad syndrome.

Authors:  Deepa Aggarwal; Kabir Sardana; Praveen Kumar; Vivek Dewan; V K Anand
Journal:  Indian J Pediatr       Date:  2004-08       Impact factor: 1.967

6.  The Sabinas syndrome.

Authors:  R R Howell; A I Arbisser; D S Parsons; C I Scott; U Fraustadt; W R Collie; R N Marshall; O C Ibarra
Journal:  Am J Hum Genet       Date:  1981-11       Impact factor: 11.025

7.  Familial hypogonadotropic hypogonadism with alopecia.

Authors:  I S Slti; Z Salem
Journal:  Can Med Assoc J       Date:  1979-08-18       Impact factor: 8.262

8.  Hypergonadotropic hypogonadism, progressive early-onset spinocerebellar ataxia, and late-onset sensorineural hearing loss: case report and literature review.

Authors:  E Sarikaya; Cg Ensert; Hc Gulerman
Journal:  Balkan J Med Genet       Date:  2011-12       Impact factor: 0.519

9.  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

10.  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
  10 in total

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