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Evolution of the phenotype in a family with an LMNA gene mutation presenting with isolated cardiac involvement.
- Source :
-
Muscle & nerve [Muscle Nerve] 2010 Jan; Vol. 41 (1), pp. 85-91. - Publication Year :
- 2010
-
Abstract
- The aim of this study is to report the evolution of a phenotype in members of a single family carrying the heterozygous exon 1 c.178 C/G, p.Arg 60 Gly LMNA gene mutation. All mutated family members underwent neurological and cardiological assessments for a period ranging from 10 to 20 years. At onset, 4 affected adult members presented a phenotype that required pacemaker implantation. Three subjects underwent cardiac transplantation leading to long-term survival in 2 of them. One of the 3 longest surviving relatives manifested late lipodystrophy, and the other 2 had lipodystrophy, insulin-resistant diabetes, and distal peripheral neuropathy. The findings demonstrate that the exon 1 c.178 C/G, p.Arg 60 Gly LMNA gene mutation is associated with a novel phenotype featuring cardiac involvement followed by late lipodystrophy, diabetes, and peripheral axonal neuropathy.
- Subjects :
- Adolescent
Adult
Cardiomyopathy, Dilated diagnosis
Cardiomyopathy, Dilated metabolism
Charcot-Marie-Tooth Disease diagnosis
Charcot-Marie-Tooth Disease genetics
Charcot-Marie-Tooth Disease metabolism
DNA Mutational Analysis
Electromyography
Exons
Female
Follow-Up Studies
Humans
Lamin Type A metabolism
Lipodystrophy diagnosis
Lipodystrophy genetics
Lipodystrophy metabolism
Magnetic Resonance Imaging
Male
Pedigree
Phenotype
Time Factors
Tomography, X-Ray Computed
Young Adult
Cardiomyopathy, Dilated genetics
DNA genetics
Family
Lamin Type A genetics
Mutation
Subjects
Details
- Language :
- English
- ISSN :
- 1097-4598
- Volume :
- 41
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Muscle & nerve
- Publication Type :
- Academic Journal
- Accession number :
- 19768759
- Full Text :
- https://doi.org/10.1002/mus.21443