Literature DB >> 2651568

Ullrich's congenital atonic sclerotic muscular dystrophy. A case report.

L De Paillette1, J Aicardi, F Goutières.   

Abstract

A 5-year old girl with Ullrich's atonic-sclerotic muscular dystrophy is reported and 16 previously reported cases are reviewed. The clinical features, in particular proximal contractures, distal hyperextensibility, mild dysmorphism and hyperhidrosis, allow recognition of this subtype of congenital muscular dystrophy, which has no specific pathological characteristics. There is evidence in favour of an autosomal recessive mode of inheritance.

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Year:  1989        PMID: 2651568     DOI: 10.1007/bf00314406

Source DB:  PubMed          Journal:  J Neurol        ISSN: 0340-5354            Impact factor:   4.849


  8 in total

1.  [Atonic sclerotic muscular dystrophy (Ullrich) in the framework of mesodermal dysplasia].

Authors:  H SCHNEIDER
Journal:  Z Orthop Ihre Grenzgeb       Date:  1957

2.  [Congenital atonic-sclerotic muscular dystrophy (Ullrich type)].

Authors:  H GOTT; E A JOSTEN
Journal:  Z Kinderheilkd       Date:  1954

3.  A case of Ullrich's disease (Kongenitale, Atonisch-Sklerotische Muskeldystrophie).

Authors:  K Nihei; S Kamoshita; T Atsumi
Journal:  Brain Dev       Date:  1979       Impact factor: 1.961

4.  Congenital muscular dystrophy: the importance of early diagnosis and orthopaedic management in the long-term prognosis.

Authors:  R Jones; R Khan; S Hughes; V Dubowitz
Journal:  J Bone Joint Surg Br       Date:  1979-02

5.  Benign congenital muscular dystrophy: a special form of congenital hypotonia.

Authors:  H Zellweger; A Afifi; W F McCormick; W Mergner
Journal:  Clin Pediatr (Phila)       Date:  1967-11       Impact factor: 1.168

6.  [Congenital muscular dystrophy].

Authors:  F Vassella; M Mumenthaler; E Rossi; H Moser; U Wiesmann
Journal:  Dtsch Z Nervenheilkd       Date:  1967

7.  Severe congenital muscular dystrophy.

Authors:  H Zellweger; A Afifi; W F McCormick; W Mergner
Journal:  Am J Dis Child       Date:  1967-12

8.  Congenital muscular dystrophy: a clinico-pathological and follow-up study of 15 patients.

Authors:  M Donner; J Rapola; H Somer
Journal:  Neuropadiatrie       Date:  1975-08
  8 in total
  3 in total

Review 1.  Collagen VI related muscle disorders.

Authors:  A K Lampe; K M D Bushby
Journal:  J Med Genet       Date:  2005-09       Impact factor: 6.318

2.  Mutations in COL6A3 cause severe and mild phenotypes of Ullrich congenital muscular dystrophy.

Authors:  Ercan Demir; Patrizia Sabatelli; Valérie Allamand; Ana Ferreiro; Behzad Moghadaszadeh; Mohamed Makrelouf; Haluk Topaloglu; Bernard Echenne; Luciano Merlini; Pascale Guicheney
Journal:  Am J Hum Genet       Date:  2002-04-24       Impact factor: 11.025

3.  New molecular mechanism for Ullrich congenital muscular dystrophy: a heterozygous in-frame deletion in the COL6A1 gene causes a severe phenotype.

Authors:  Te-Cheng Pan; Rui-Zhu Zhang; Dominick G Sudano; Suely K Marie; Carsten G Bönnemann; Mon-Li Chu
Journal:  Am J Hum Genet       Date:  2003-07-01       Impact factor: 11.025

  3 in total

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