PedAM

Pediatric Disease Annotations & Medicines

Disease	dilated cardiomyopathy
Phenotype	C0026850\|muscular dystrophy
Sentences	11
PubMedID- 22077867	Osteopontin--a fibrosis-related marker--in dilated cardiomyopathy in patients with emery-dreifuss muscular dystrophy.
PubMedID- 24996370	A novel dystrophin deletion mutation in a becker muscular dystrophy patient with early-onset dilated cardiomyopathy.
PubMedID- 23418438	The homozygous mice develop, similarly to human patients, progressive muscular dystrophy associated with dilated cardiomyopathy [31].
PubMedID- 22427904	Mutations in dysferlin cause muscular dystrophy, but development of dilated cardiomyopathy is rare [96], [97].
PubMedID- 20182615	These diseases include dilated cardiomyopathy with variable muscular dystrophy, dunnigan-type familial partial lipodystrophy, a charcot-marie-tooth type 2 disease, mandibuloacral dysplasia, and hutchinson-gilford progeria syndrome.
PubMedID- 20501885	The duchenne and becker forms of muscular dystrophy are associated with dilated cardiomyopathy and are diseases in which pulmonary function peaks and then progressively declines.
PubMedID- 23933734	Mutations in the lamin a/c gene (lmna) encoding a-type nuclear lamins cause dilated cardiomyopathy with variable muscular dystrophy.
PubMedID- 23400933	A dilated cardiomyopathy (dcm) is associated with duchenne muscular dystrophy (dmd).
PubMedID- 20497525	Kuru et al[3] reported a 57-year-old japanese woman with dysferlinopathy manifested as secondary dilated cardiomyopathy attributable to muscular dystrophy.
PubMedID- 23048029	Mutations in the lamin a/c gene (lmna) cause a diverse spectrum of diseases, the most common of which is dilated cardiomyopathy often with skeletal muscular dystrophy.
PubMedID- 22655514	However carvedilol therapy can be safe for patients with dilated cardiomyopathy associated with muscular dystrophy, even producing a modest improvement in systolic and diastolic function (26).

Page: 1