| Literature DB >> 8481038 |
W Reardon1, R Newcombe, I Fenton, J Sibert, P S Harper.
Abstract
Although the genetic basis of the congenital form of myotonic dystrophy has recently been clarified, data as to outcome in terms of life expectancy and morbidity are scanty. Life table data based on a cohort of 115 patients with a confirmed diagnosis of congenital myotonic dystrophy are presented. The data suggest a 25% chance of death before 18 months of age and a 50% chance of survival into the mid-30s. The profile of disease and complications among survivors is also charted.Entities:
Mesh:
Year: 1993 PMID: 8481038 PMCID: PMC1029229 DOI: 10.1136/adc.68.2.177
Source DB: PubMed Journal: Arch Dis Child ISSN: 0003-9888 Impact factor: 3.791