Literature DB >> 8211986

Autopsy analyses of the muscular dystrophies.

T Moriuchi1, N Kagawa, M Mukoyama, K Hizawa.   

Abstract

Life span, causes of death, weight of heart, liver, brain, and main pathological changes of internal organs were analysed on 329 autopsy cases of muscular dystrophies. These included 249 cases of Duchenne muscular dystrophy (DMD), 3 Becker muscular dystrophies (BMD), 14 limb-girdle muscular dystrophies (LGMD), 3 fascioscapulohumeral muscular dystrophies (FSH), 18 Fukuyama type congenital muscular dystrophies (FCMD) and 17 myotonic dystrophies (MyD). In DMD the life span has definitely prolonged in recent years. Pulmonary infection, which was once the major cause of death, has greatly decreased in recent years. Instead, respiratory and cardiac failures caused by dystrophic changes of respiratory and cardiac muscles were more closely related to the causes of death in many recent cases. Myocardial fibrosis was observed in most of the patients with DMD, BMD, LGMD, FCMD and MyD. The distribution of cardiac lesions was similar in BMD, LGMD and FCMD as in DMD. In MyD the disorders involved more frequently conductive muscles resulting in arrhythmias. The dystrophic cardiomyopathy seemed to be a part of the essential changes in all types of muscular dystrophy, although different in intensity and rate of morbidity. Alzheimer's neurofibrillary changes were observed in the brain of some cases of FCMD and MyD, suggesting the possibility of precocious aging of the brain in some patients of the muscular dystrophies.

Entities:  

Mesh:

Year:  1993        PMID: 8211986

Source DB:  PubMed          Journal:  Tokushima J Exp Med        ISSN: 0040-8875


  27 in total

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Review 3.  Viral-mediated gene therapy for the muscular dystrophies: successes, limitations and recent advances.

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4.  Increased connective tissue growth factor associated with cardiac fibrosis in the mdx mouse model of dystrophic cardiomyopathy.

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5.  [Facioscapulohumeral muscle dystrophy and heart disease].

Authors:  P Emmrich; V Ogunlade; T Gradistanac; S Daneschnejad; M C Koch; R Schober
Journal:  Z Kardiol       Date:  2005-05

6.  Chronic administration of membrane sealant prevents severe cardiac injury and ventricular dilatation in dystrophic dogs.

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7.  Adeno-Associated Virus-Mediated Delivery of CRISPR for Cardiac Gene Editing in Mice.

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Journal:  J Vis Exp       Date:  2018-08-02       Impact factor: 1.355

8.  Arginine metabolism by macrophages promotes cardiac and muscle fibrosis in mdx muscular dystrophy.

Authors:  Michelle Wehling-Henricks; Maria C Jordan; Tomomi Gotoh; Wayne W Grody; Kenneth P Roos; James G Tidball
Journal:  PLoS One       Date:  2010-05-21       Impact factor: 3.240

9.  Abnormal circumferential strain is present in young Duchenne muscular dystrophy patients.

Authors:  Thomas D Ryan; Michael D Taylor; Wojciech Mazur; Linda H Cripe; Jesse Pratt; Eileen C King; Kathleen Lao; Michelle A Grenier; John L Jefferies; D Woodrow Benson; Kan N Hor
Journal:  Pediatr Cardiol       Date:  2013-01-29       Impact factor: 1.655

Review 10.  Cardiac involvement in Duchenne and Becker muscular dystrophy.

Authors:  Sophie Mavrogeni; George Markousis-Mavrogenis; Antigoni Papavasiliou; Genovefa Kolovou
Journal:  World J Cardiol       Date:  2015-07-26
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