Literature DB >> 474619

The G syndrome: a case report.

C R Greenberg, D Schraufnagel.   

Abstract

A case of the G syndrome is reported in a baby boy who had an unusual facies (prominent forehead, telecanthus, posteriorly rotated ears, and anteverted nostrils), laryngeal cleft, hypospadias, cryptorchidism, and psychomotor development delay, possibly secondary to birth asphyxia and numerous medical and surgical complications. The mother had a similar facies.

Entities:  

Mesh:

Year:  1979        PMID: 474619     DOI: 10.1002/ajmg.1320030111

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


  2 in total

1.  Further delineation of the G syndrome: a manageable genetic cause of infantile dysphagia.

Authors:  G N Wilson; W J Oliver
Journal:  J Med Genet       Date:  1988-03       Impact factor: 6.318

2.  Congenital alacrima in a patient with G (Opitz Frias) syndrome.

Authors:  M Dundar; K Erkihç; F Demiryilmaz; M Küçükaydin; M Kendirci; H Okur; A Kazez
Journal:  Hum Genet       Date:  1996-04       Impact factor: 4.132

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.