Literature DB >> 2685312

Emery-Dreifuss syndrome.

A E Emery1.   

Abstract

Emery-Dreifuss muscular dystrophy is characterised by the triad of (1) early contractures of the elbows, Achilles tendons, and postcervical muscles; (2) slowly progressive muscle wasting and weakness with a humeroperoneal distribution in the early stages; and (3) a cardiomyopathy usually presenting as heart block. The early recognition of the condition is essential because the insertion of a cardiac pacemaker can be life saving. The disorder is usually inherited as an X linked recessive trait (linked to DNA markers around Xq28). However, occasionally it can be inherited as an autosomal dominant trait and there is an indication that this and the X linked form may in some cases have a neurogenic basis. For these reasons it has recently been proposed that the appellation 'Emery-Dreifuss syndrome' be used for this triad of symptoms and signs.

Entities:  

Mesh:

Year:  1989        PMID: 2685312      PMCID: PMC1015715          DOI: 10.1136/jmg.26.10.637

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  33 in total

1.  [A new x-chromosomal muscular dystrophy].

Authors:  P E BECKER; F KIENER
Journal:  Arch Psychiatr Nervenkr Z Gesamte Neurol Psychiatr       Date:  1955

2.  Scapuloperoneal muscular atrophy with cardiopathy. An X-linked recessive trait.

Authors:  S Mawatari; K Katayama
Journal:  Arch Neurol       Date:  1973-01

3.  X-linked pseudohypertrophic muscular dystrophy with a late onset and slow progression.

Authors:  C C Mabry; I E Roeckel; R L Munich; D Robertson
Journal:  N Engl J Med       Date:  1965-11-11       Impact factor: 91.245

4.  Adult onset scapuloperoneal myopathy.

Authors:  P K Thomas; G D Schott; J A Morgan-Hughes
Journal:  J Neurol Neurosurg Psychiatry       Date:  1975-10       Impact factor: 10.154

5.  Emery-Dreifuss muscular dystrophy.

Authors:  R P Dickey; F A Ziter; R A Smith
Journal:  J Pediatr       Date:  1984-04       Impact factor: 4.406

6.  Atrioventricular block and supraventricular arrhythmias with X-linked muscular dystrophy.

Authors:  Z ul Hassan; C P Fastabend; P K Mohanty; E R Isaacs
Journal:  Circulation       Date:  1979-12       Impact factor: 29.690

7.  Scapuloperoneal syndrome with cardiomyopathy: report of a family with autosomal dominant inheritance and unusual features.

Authors:  A Chakrabarti; J M Pearce
Journal:  J Neurol Neurosurg Psychiatry       Date:  1981-12       Impact factor: 10.154

8.  Emery-dreifuss humeroperoneal muscular dystrophy: an x-linked myopathy with unusual contractures and bradycardia.

Authors:  L C Hopkins; J A Jackson; L J Elsas
Journal:  Ann Neurol       Date:  1981-09       Impact factor: 10.422

9.  Emery-Dreifuss muscular dystrophy.

Authors:  L P Rowland; M Fetell; M Olarte; A Hays; N Singh; F E Wanat
Journal:  Ann Neurol       Date:  1979-02       Impact factor: 10.422

10.  A genetic variant of Emery-Dreifuss disease. Muscular dystrophy with humeropelvic distribution, early joint contracture, and permanent atrial paralysis.

Authors:  K Takamoto; K Hirose; M Uono; I Nonaka
Journal:  Arch Neurol       Date:  1984-12
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  26 in total

1.  Emery-Dreifuss muscular dystrophy in the evaluation of decreased spinal mobility and joint contractures.

Authors:  Kamil Goncu; Rengin Guzel; Fusun Guler-Uysal
Journal:  Clin Rheumatol       Date:  2003-10-21       Impact factor: 2.980

Review 2.  The muscular dystrophies: from genes to therapies.

Authors:  Richard M Lovering; Neil C Porter; Robert J Bloch
Journal:  Phys Ther       Date:  2005-12

Review 3.  Diseases of the Nucleoskeleton.

Authors:  James M Holaska
Journal:  Compr Physiol       Date:  2016-09-15       Impact factor: 9.090

Review 4.  Gathering up meiotic telomeres: a novel function of the microtubule-organizing center.

Authors:  Ayumu Yamamoto
Journal:  Cell Mol Life Sci       Date:  2014-01-11       Impact factor: 9.261

5.  A cross section of autosomal recessive limb-girdle muscular dystrophies in 38 families.

Authors:  P Dinçer; Z Akçören; E Demir; I Richard; O Sancak; G Kale; S Ozme; A Karaduman; E Tan; J A Urtizberea; J S Beckmann; H Topaloğlu
Journal:  J Med Genet       Date:  2000-05       Impact factor: 6.318

6.  Different mutations in the LMNA gene cause autosomal dominant and autosomal recessive Emery-Dreifuss muscular dystrophy.

Authors:  M Raffaele Di Barletta; E Ricci; G Galluzzi; P Tonali; M Mora; L Morandi; A Romorini; T Voit; K H Orstavik; L Merlini; C Trevisan; V Biancalana; I Housmanowa-Petrusewicz; S Bione; R Ricotti; K Schwartz; G Bonne; D Toniolo
Journal:  Am J Hum Genet       Date:  2000-03-16       Impact factor: 11.025

Review 7.  Multiple pathogenetic mechanisms in X linked dilated cardiomyopathy.

Authors:  N Cohen; F Muntoni
Journal:  Heart       Date:  2004-08       Impact factor: 5.994

Review 8.  Anti-cardiac troponin antibodies in clinical human disease: a systematic review.

Authors:  Eduardo M Vilela; Rita Bettencourt-Silva; J Torres da Costa; Ana Raquel Barbosa; Marisa P Silva; Madalena Teixeira; João Primo; Vasco Gama Ribeiro; José Pedro L Nunes
Journal:  Ann Transl Med       Date:  2017-08

Review 9.  Emerin in health and disease.

Authors:  Adam J Koch; James M Holaska
Journal:  Semin Cell Dev Biol       Date:  2013-12-21       Impact factor: 7.727

10.  Emery-Dreifuss muscular dystrophy: linkage to markers in distal Xq28.

Authors:  J R Yates; J P Warner; J A Smith; F Deymeer; J P Azulay; I Hausmanowa-Petrusewicz; J Zaremba; J Borkowska; N A Affara; M A Ferguson-Smith
Journal:  J Med Genet       Date:  1993-02       Impact factor: 6.318

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