Literature DB >> 4073118

A family with the Saethre-Chotzen syndrome.

E Bianchi, M Aricŏ, A F Podestă, M Grana, P Fiori, G Beluffi.   

Abstract

Acrocephalosyndactyly (ACS) is an inherited syndrome of premature synostosis of the cranial sutures and abnormalities in the distal segments of the limbs. Several forms of ACS have been described. ACS type III (or Saethre-Chotzen syndrome) is characterized by microcephaly, skull asymmetry, mild syndactyly, and facial abnormalities. We describe an Italian family with ACS III in which two sibs are clearly affected; the mother and the maternal grandmother show some features of the syndrome.

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Year:  1985        PMID: 4073118     DOI: 10.1002/ajmg.1320220402

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


  1 in total

1.  Saethre-Chotzen syndrome: a clinical, EEG and neuroradiological study.

Authors:  M Elia; S A Musumeci; R Ferri; D Greco; C Romano; S Del Gracco; M C Stefanini
Journal:  Childs Nerv Syst       Date:  1996-11       Impact factor: 1.475

  1 in total

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