| Literature DB >> 6424376 |
H O Akesson, R Axelsson, B Samuelsson.
Abstract
A case report is given of a pair of monozygotic twin girls with neurofibromatosis caused by a new mutation. The symptomatology was dominated by a neurofibrosarcoma on the leg of one twin and by a large plexiform neurofibroma on the neck of the other twin. Otherwise, the disease showed similar, although not identical or mirror-image distribution of subcutaneous neurofibromas and café-au-lait spots. The twins had identical HLA and blood group antigens and the same chromosome aberration. These case reports indicate that nonhereditary factors may influence the manifestations of neurofibromatosis. A review of the literature on monozygotic twins with neurofibromatosis is given.Entities:
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Year: 1983 PMID: 6424376 DOI: 10.1017/s0001566000005109
Source DB: PubMed Journal: Acta Genet Med Gemellol (Roma) ISSN: 0001-5660