doi: 10.1016/0002-9343(76)90764-6.
Multiple lentigines syndrome. Case report and review of the literature
- PMID: 1258892
- DOI: 10.1016/0002-9343(76)90764-6
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Multiple lentigines syndrome. Case report and review of the literature
Am J Med.
1976 Mar.
Abstract
The multiple lentigines syndrome is reviewed and a new case is presented. The major features of this syndrome are lentigines and other cutaneous abnormalities, cardiac defects, meurologic defects, cephalofacila dysmorphism, shortness of stature, skeletal anomalies, genitourinary abnormalities, and a family history consistent with an autosomal dominant mode of inheritance. The multiple lentigines syndrome manifests markedly variable expressivity; no single finding is pathognomonic and few patients have all major features. We propose specific criteria for diagnosis.
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