Literature DB >> 2596515

Autosomal recessive form of whistling face syndrome in sibs.

B Dallapiccola1, A Giannotti, A Lembo, L Saguì.   

Abstract

Two sibs with the whistling face syndrome, born to unaffected parents, are presented. They had the full facial and limb manifestations typical of this disorder, for which there is evidence of autosomal dominant inheritance. The existence of an autosomal recessive form of this syndrome has been suspected previously on the basis of a limited number of observations. Our study substantiates genetic heterogeneity of this condition and suggests that the autosomal recessive form could be even less rare than is generally considered.

Entities:  

Mesh:

Year:  1989        PMID: 2596515     DOI: 10.1002/ajmg.1320330426

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


  3 in total

Review 1.  Freeman-sheldon syndrome presenting with microstomia: a case report and literature review.

Authors:  Vivek Gurjar; Anita Parushetti; Minal Gurjar
Journal:  J Maxillofac Oral Surg       Date:  2012-05-17

Review 2.  Freeman-Sheldon syndrome. A case report and review of the literature.

Authors:  Daniele Ferrari; Camilla Bettuzzi; Onofrio Donzelli
Journal:  Chir Organi Mov       Date:  2008-08-01

3.  Freeman-Sheldon Syndrome: First Molecularly Confirmed Case from Sub-Saharan Africa.

Authors:  A M Ali; R M Mbwasi; G Kinabo; E-J Kamsteeg; B C Hamel; M C J Dekker
Journal:  Case Rep Genet       Date:  2017-05-11
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.