Literature DB >> 3612171

Emery-Dreifuss muscular dystrophy. An autopsy case.

H Hara, H Nagara, S Mawatari, A Kondo, H Sato.   

Abstract

We reported the autopsy findings in a 50-year-old man with typical clinical features of Emery-Dreifuss muscular dystrophy. Special attention was directed to the spinal cord and ventral spinal roots to determine whether cause of the muscle wasting was denervation or myopathy. Neuropathological studies disclosed no abnormality of the spinal cord, and the ventral spinal roots were intact. The skeletal muscles showed dystrophic changes of varying degrees, and marked cardiomyopathy was evident. We consider that muscle wasting in this man was due to muscular dystrophy.

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Year:  1987        PMID: 3612171     DOI: 10.1016/0022-510x(87)90256-5

Source DB:  PubMed          Journal:  J Neurol Sci        ISSN: 0022-510X            Impact factor:   3.181


  3 in total

1.  Autosomal dominant Emery-Dreifuss syndrome: evidence of a neurogenic variant of the disease.

Authors:  T N Witt; C G Garner; D Pongratz; X Baur
Journal:  Eur Arch Psychiatry Neurol Sci       Date:  1988

Review 2.  Emery-Dreifuss syndrome.

Authors:  A E Emery
Journal:  J Med Genet       Date:  1989-10       Impact factor: 6.318

3.  X-Linked Emery-Dreifuss Muscular Dystrophy: Study Of X-Chromosome Inactivation and Its Relation with Clinical Phenotypes in Female Carriers.

Authors:  Emanuela Viggiano; Agnieszka Madej-Pilarczyk; Nicola Carboni; Esther Picillo; Manuela Ergoli; Stefania Del Gaudio; Michal Marchel; Gerardo Nigro; Alberto Palladino; Luisa Politano
Journal:  Genes (Basel)       Date:  2019-11-11       Impact factor: 4.096

  3 in total

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