Literature DB >> 8484414

Bone dysplasia, midface hypoplasia, and deafness: three new patients and review of the literature.

H Kääriäinen1, M Barrow, R Hennekam.   

Abstract

We report on 3 unrelated patients with a syndrome of sensorineural deafness (3/3), midface hypoplasia (3/3), disproportionate shortness with short limbs (3/3), cleft palate or bifid uvula (3/3), and lack of high myopia (3/3). This brings the number of reported patients with this condition to 11. Different names such as oto-spondylo-megaepiphyseal dysplasia (OSMED) or the Insley-Astley syndrome have been used. We propose the name "syndrome of bone dysplasia, midface hypoplasia, and deafness" which lists the 3 main manifestations of the condition.

Entities:  

Mesh:

Year:  1993        PMID: 8484414     DOI: 10.1002/ajmg.1320460224

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


  3 in total

1.  A type II collagen mutation also results in oto-spondylo-megaepiphyseal dysplasia.

Authors:  Yoshinari Miyamoto; Eiji Nakashima; Hisatada Hiraoka; Hirofumi Ohashi; Shiro Ikegawa
Journal:  Hum Genet       Date:  2005-11-15       Impact factor: 4.132

2.  Autosomal recessive disorder otospondylomegaepiphyseal dysplasia is associated with loss-of-function mutations in the COL11A2 gene.

Authors:  M Melkoniemi; H G Brunner; S Manouvrier; R Hennekam; A Superti-Furga; H Kääriäinen; R M Pauli; T van Essen; M L Warman; J Bonaventure; P Miny; L Ala-Kokko
Journal:  Am J Hum Genet       Date:  2000-02       Impact factor: 11.025

3.  Mental retardation - megaepiphyses - ulnar pseudoepiphyses - hypoplastic fibulae - brachymesophalangia: a new syndrome.

Authors:  G Nishimura; K Kozlowski; K Tachibana; K Kameshita; S Ohba
Journal:  Pediatr Radiol       Date:  1996
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.