Literature DB >> 8488880

Oral-facial-digital syndrome type I in a newborn male.

Y Gillerot1, M Heimann, C Fourneau, C Verellen-Dumoulin, L Van Maldergem.   

Abstract

We report on a newborn male, born at term with clinical manifestations of oral-facial-digital (OFD) syndrome type I. This syndrome is generally assumed to be inherited in an X-linked dominant fashion with lethality in males. Therefore, liveborn males are exceptional. This liveborn male also had Dandy-Walker malformation and polycystic kidneys. From a general point of view, distinction between the 8 types of OFD syndromes described so far appears subtle and considerable overlap exists between them. In this regard, it should be noted that polycystic kidneys different from adult polycystic kidney disease both macroscopically and microscopically are a frequent manifestation of OFD I.

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Year:  1993        PMID: 8488880     DOI: 10.1002/ajmg.1320460318

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


  6 in total

1.  Clinical, molecular, and genotype-phenotype correlation studies from 25 cases of oral-facial-digital syndrome type 1: a French and Belgian collaborative study.

Authors:  C Thauvin-Robinet; M Cossée; V Cormier-Daire; L Van Maldergem; A Toutain; Y Alembik; E Bieth; V Layet; P Parent; A David; A Goldenberg; G Mortier; D Héron; P Sagot; A M Bouvier; F Huet; V Cusin; A Donzel; D Devys; J R Teyssier; L Faivre
Journal:  J Med Genet       Date:  2006-01       Impact factor: 6.318

Review 2.  Oral and craniofacial clinical signs associated to genetic conditions in human identification part I: a review.

Authors:  Fouad Ayoub; Nicole Aoun; Hassan El Husseini; Houssam Jassar; Fida Sayah; Ziad Salameh
Journal:  J Int Oral Health       Date:  2015-05

3.  Oral-facial-digital syndrome type 1 in males: Congenital heart defects are included in its phenotypic spectrum.

Authors:  Arjan Bouman; Mariëlle Alders; Roelof Jan Oostra; Elisabeth van Leeuwen; Nikki Thuijs; Anne-Marie van der Kevie-Kersemaekers; Merel van Maarle
Journal:  Am J Med Genet A       Date:  2017-04-03       Impact factor: 2.802

4.  Distinctive Skeletal Abnormalities With No Microdeletions or Microduplications on Array-CGH in a Boy With Mohr Syndrome (Oro-Facial-Digital Type II).

Authors:  Ali Al Kaissi; Renata Pospischill; Franz Grill; Rudolf Ganger
Journal:  J Clin Med Res       Date:  2015-10-23

5.  An Atypical Presentation of a Male with Oral-Facial-Digital Syndrome Type 1 Related Ciliopathy.

Authors:  Sheena Sharma; Jennifer M Kalish; Ethan M Goldberg; Francis Jeshira Reynoso; Madhura Pradhan
Journal:  Case Rep Nephrol       Date:  2016-08-29

6.  Comprehensive prosthetic rehabilitation of a case of the orofacial digital syndrome.

Authors:  Rajat Lanzara; M Viswambaran; Anup Gopi
Journal:  J Indian Prosthodont Soc       Date:  2020-01-27
  6 in total

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