Literature DB >> 7153059

Oto-spondylo-megaepiphyseal dysplasia (OSMED).

A Giedion, M Brandner, J Lecannellier, U Muhar, A Prader, J Sulzer, E Zweymüller.   

Abstract

Four personal longitudinal observations and two cases from the literature are used to introduce the concept of oto-spondylo-megaepiphyseal dysplasia (OSMED). The condition may be recognized at birth. The main clinical findings are sensoneurinal deafness, enlarged 1st interphalangeal joints of the hands, relative short extremities with abnormally large knees and elbows but still normal total body length. In the second decade of life, backpain and decreased mobility of the joints may follow. 4/6 patients had a cleft palate. The diagnostic radiological findings are the big epiphyses combined with a moderate platyspondyly, most marked in the lower thoracic region. The occurrence of OSMED in two sisters suggests an autosomal-recessive transmission. No biochemical anomaly could be detected.

Entities:  

Mesh:

Year:  1982        PMID: 7153059

Source DB:  PubMed          Journal:  Helv Paediatr Acta        ISSN: 0018-022X


  11 in total

Review 1.  International classification of osteochondrodysplasias. The International Working Group on Constitutional Diseases of Bone.

Authors:  J Spranger
Journal:  Eur J Pediatr       Date:  1992-06       Impact factor: 3.183

2.  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

3.  Audiological findings in otospondylomegaepiphyseal dysplasia (OSMED) associated with a novel mutation in COL11A2.

Authors:  Suna Tokgöz-Yılmaz; Sanem Sahlı; Suat Fitoz; Gonca Sennaroğlu; Mustafa Tekin
Journal:  Int J Pediatr Otorhinolaryngol       Date:  2011-01-03       Impact factor: 1.675

Review 4.  Clinical and Molecular genetics of Stickler syndrome.

Authors:  M P Snead; J R Yates
Journal:  J Med Genet       Date:  1999-05       Impact factor: 6.318

Review 5.  The type II collagenopathies: a spectrum of chondrodysplasias.

Authors:  J Spranger; A Winterpacht; B Zabel
Journal:  Eur J Pediatr       Date:  1994-02       Impact factor: 3.183

6.  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

7.  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

8.  Macroepiphyseal dysplasia with symptomatic osteoporosis, wrinkled skin, and aged appearance: a presumed autosomal recessive condition.

Authors:  W H McAlister; J D Coe; M P Whyte
Journal:  Skeletal Radiol       Date:  1986       Impact factor: 2.199

9.  Spondylo-megaepiphyseal-metaphyseal dysplasia: an unusual bone dysplasia.

Authors:  Prachi Pragya Agarwal; Ashok Srinivasan; Raju Sharma; Madhulika Kabra; Arun Kumar Gupta
Journal:  Pediatr Radiol       Date:  2003-09-06

10.  Total Hip Arthroplasty in a Patient with Oto-Spondylo-Megaepiphyseal Dysplasia Planned by Three-Dimensional Motion Analyses and Full-Scale Three-Dimensional Plaster Model of Bones.

Authors:  Takeyuki Tanaka; Hideya Ito; Hirofumi Oshima; Nobuhiko Haga; Sakae Tanaka
Journal:  Case Rep Orthop       Date:  2018-01-23
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