Literature DB >> 702237

The phenotypic variability of diastrophic dysplasia.

W A Horton, D L Rimoin, R S Lachman, F Skovby, D W Hollister, J Spranger, C I Scott, J G Hall.   

Abstract

To determine the relationship between so-called "diastrophic variant" and diastrophic dysplasia, four patients considered to have the variant condition were studied in detail and compared to 67 patients (including 17 sets of affected sibs) considered to have classical diastrophic dysplasia. Analysis of the combined clinical, radiographic, histologic, and genetic data indicates that there is wide variability in the phenotypic expression of diastrophic dysplasia, even within sibships, and that those individuals previously labeled as having "diastrophic variant" appear to have mild diastrophic dysplasia.

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Year:  1978        PMID: 702237     DOI: 10.1016/s0022-3476(78)80896-8

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


  10 in total

Review 1.  The Finnish Disease Heritage III: the individual diseases.

Authors:  Reijo Norio
Journal:  Hum Genet       Date:  2003-03-08       Impact factor: 4.132

2.  Diastrophic dysplasia: a case report.

Authors:  L Mehta; I C Verma; J P Soni; R U Singhania
Journal:  Indian J Pediatr       Date:  1992 Nov-Dec       Impact factor: 1.967

3.  Exclusion of the COL2A1 gene as the mutation site in diastrophic dysplasia.

Authors:  K Elima; I Kaitila; L Mikonoja; U Elonsalo; L Peltonen; E Vuorio
Journal:  J Med Genet       Date:  1989-05       Impact factor: 6.318

4.  Matrix disruptions, growth, and degradation of cartilage with impaired sulfation.

Authors:  Edward L Mertz; Marcella Facchini; Anna T Pham; Benedetta Gualeni; Fabio De Leonardis; Antonio Rossi; Antonella Forlino
Journal:  J Biol Chem       Date:  2012-05-03       Impact factor: 5.157

5.  Unilateral hyperplasia of the left posterior arch and associated vertebral schisis at C6 level.

Authors:  Giuseppe Esposito; Pasquale de Bonis; Gianpiero Tamburrini; Luca Massimi; Vadim Byvaltsev; Concezio di Rocco; Antonio Leone
Journal:  Skeletal Radiol       Date:  2009-07-25       Impact factor: 2.199

6.  Atelosteogenesis type II is caused by mutations in the diastrophic dysplasia sulfate-transporter gene (DTDST): evidence for a phenotypic series involving three chondrodysplasias.

Authors:  J Hästbacka; A Superti-Furga; W R Wilcox; D L Rimoin; D H Cohn; E S Lander
Journal:  Am J Hum Genet       Date:  1996-02       Impact factor: 11.025

7.  Cartilage-hair hypoplasia--clinical manifestations in 108 Finnish patients.

Authors:  O Mäkitie; I Kaitila
Journal:  Eur J Pediatr       Date:  1993-03       Impact factor: 3.183

8.  Lipid storage myopathy associated with scoliosis and multiple joint contractures.

Authors:  H Nogami; N Ogasawara; T Kasai; T Oki; S Murachi
Journal:  Acta Neuropathol       Date:  1983       Impact factor: 17.088

9.  Morphologic studies in the skeletal dysplasias.

Authors:  D O Sillence; W A Horton; D L Rimoin
Journal:  Am J Pathol       Date:  1979-09       Impact factor: 4.307

10.  Diastrophic dysplasia gene maps to the distal long arm of chromosome 5.

Authors:  J Hästbacka; I Kaitila; P Sistonen; A de la Chapelle
Journal:  Proc Natl Acad Sci U S A       Date:  1990-10       Impact factor: 11.205

  10 in total

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