Literature DB >> 8261648

Oral-facial-digital syndrome with fibular aplasia: a new variant.

L E Figuera1, F Rivas, J M Cantú.   

Abstract

The oral-facial-digital (OFD) syndromes constitute a heterogeneous group of entities usually associated with certain features that permit a specific diagnosis. This report refers to a 10-month-old girl with cleft palate, mesomelic limb shortening, oligopolydactyly, and fibular aplasia. Since this combination has not been described previously, it is proposed as a distinct type of oral-facial-digital syndrome, and we suggest mutations of homeotic genes to explain some abnormalities present in the OFD syndromes.

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Year:  1993        PMID: 8261648     DOI: 10.1111/j.1399-0004.1993.tb03877.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  5 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

2.  C5orf42 is the major gene responsible for OFD syndrome type VI.

Authors:  Estelle Lopez; Christel Thauvin-Robinet; Bruno Reversade; Nadia El Khartoufi; Louise Devisme; Muriel Holder; Hélène Ansart-Franquet; Magali Avila; Didier Lacombe; Pascale Kleinfinger; Irahara Kaori; Jun-Ichi Takanashi; Martine Le Merrer; Jelena Martinovic; Catherine Noël; Mohammad Shboul; Lena Ho; Yeliz Güven; Ferechté Razavi; Lydie Burglen; Nadège Gigot; Véronique Darmency-Stamboul; Julien Thevenon; Bernard Aral; Hülya Kayserili; Frédéric Huet; Stanislas Lyonnet; Cédric Le Caignec; Brunella Franco; Jean-Baptiste Rivière; Laurence Faivre; Tania Attié-Bitach
Journal:  Hum Genet       Date:  2013-11-01       Impact factor: 4.132

3.  A Japanese male patient with 'fibular aplasia, tibial campomelia and oligodactyly': an additional case report.

Authors:  Taichi Kitaoka; Noriyuki Namba; Ji Yoo Kim; Takuo Kubota; Kohji Miura; Yoko Miyoshi; Haruhiko Hirai; Mikihiko Kogo; Keiichi Ozono
Journal:  Clin Pediatr Endocrinol       Date:  2009-08-01

Review 4.  Update on oral-facial-digital syndromes (OFDS).

Authors:  Brunella Franco; Christel Thauvin-Robinet
Journal:  Cilia       Date:  2016-05-02

Review 5.  Clinical and genetic heterogeneity of primary ciliopathies (Review).

Authors:  Ina Ofelia Focșa; Magdalena Budișteanu; Mihaela Bălgrădean
Journal:  Int J Mol Med       Date:  2021-07-19       Impact factor: 4.101

  5 in total

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