Literature DB >> 6683357

Prospective study of X-linked progressive muscular dystrophy in Campania.

G Nigro, L I Comi, F M Limongelli, M A Giugliano, L Politano, V Petretta, L Passamano, S Stefanelli.   

Abstract

Within the Campania region of southern Italy a prospective study on X-linked progressive muscular dystrophy was conducted over a period of 12 years from 1969 to 1980, inclusive. The mean incidence rate was 21.7 per 100,000 male livebirths for Duchenne muscular dystrophy (DMD) cases and 3.2 per 100,000 male livebirths for Becker muscular dystrophy (BMD) cases. The familial cases were 38.5% among the DMD patients and 50% among the BMD patients. Myocardial involvement appeared in DMD patients at about 6 years of age in a high percentage of cases and increased progressively until the last years of life, when cardiac damage occurred in 95% of cases. The percentage of myocardial involvement in BMD patients was very low before 13 years of age, but increased progressively until 20 years, when cardiac damage occurred in 80% of cases studied; severe cardiomyopathy did not occur before the age of 21. The data reported also include the effects of age on physical performance, serum creatine kinase activity and serum myoglobin levels, the types of cardiac damage, and the causes of death.

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Year:  1983        PMID: 6683357     DOI: 10.1002/mus.880060403

Source DB:  PubMed          Journal:  Muscle Nerve        ISSN: 0148-639X            Impact factor:   3.217


  20 in total

1.  Phenotype-genotype analysis of dystrophinopathy caused by duplication mutation in Dystrophin gene in an African patient.

Authors:  L R Peddareddygari; B H Pillai; D Nochlin; L R Sharer; R P Grewal
Journal:  Afr Health Sci       Date:  2011-12       Impact factor: 0.927

2.  Development of Duchenne-type cardiomyopathy. Morphologic studies in a canine model.

Authors:  B A Valentine; J F Cummings; B J Cooper
Journal:  Am J Pathol       Date:  1989-10       Impact factor: 4.307

3.  Cardiovascular Complications of Neuromuscular Disorders.

Authors:  Bhavesh Sachdev; Perry M. Elliott; William J. McKenna
Journal:  Curr Treat Options Cardiovasc Med       Date:  2002-04

Review 4.  Alterations in mitochondrial function as a harbinger of cardiomyopathy: lessons from the dystrophic heart.

Authors:  Yan Burelle; Maya Khairallah; Alexis Ascah; Bruce G Allen; Christian F Deschepper; Basil J Petrof; Christine Des Rosiers
Journal:  J Mol Cell Cardiol       Date:  2009-09-18       Impact factor: 5.000

5.  A case of Becker muscular dystrophy with early manifestation of cardiomyopathy.

Authors:  Ki Hyun Doo; Hye Won Ryu; Seung Soo Kim; Byung Chan Lim; Hui Hwang; Ki Joong Kim; Yong Seung Hwang; Jong-Hee Chae
Journal:  Korean J Pediatr       Date:  2012-09-14

6.  The heart in muscular dystrophy: an electrocardiographic and ultrasound study of 20 patients.

Authors:  P Berlit; B Stegaru-Hellring
Journal:  Eur Arch Psychiatry Clin Neurosci       Date:  1991       Impact factor: 5.270

Review 7.  Cardiac involvement in Becker muscular dystrophy.

Authors:  Josef Finsterer; Claudia Stöllberger
Journal:  Can J Cardiol       Date:  2008-10       Impact factor: 5.223

8.  Birth and population prevalence of Duchenne muscular dystrophy in The Netherlands.

Authors:  A J van Essen; H F Busch; G J te Meerman; L P ten Kate
Journal:  Hum Genet       Date:  1992-01       Impact factor: 4.132

Review 9.  Duchenne and Becker Muscular Dystrophies: A Review of Animal Models, Clinical End Points, and Biomarker Quantification.

Authors:  Kristin Wilson; Crystal Faelan; Janet C Patterson-Kane; Daniel G Rudmann; Steven A Moore; Diane Frank; Jay Charleston; Jon Tinsley; G David Young; Anthony J Milici
Journal:  Toxicol Pathol       Date:  2017-10-03       Impact factor: 1.902

10.  Becker muscular dystrophy presenting with complete heart block in the sixth decade.

Authors:  R Quinlivan; J Ball; M Dunckley; D J Thomas; F Flinter; J Morgan-Hughes
Journal:  J Neurol       Date:  1995-06       Impact factor: 4.849

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