Cowden syndrome and Lhermitte-Duclos disease in a family: a single genetic syndrome with pleiotropy?

Cowden syndrome is an autosomal dominant condition of multiple hamartomas. Patients with this phakomatosis have an increased risk of breast cancer and thyroid tumours. Lhermitte-Duclos disease is usually a sporadic condition of cerebellar ganglion cell hypertrophy, ataxia, mental retardation, and se...

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Hlavní autoři: Eng, C, Murday, V, Seal, S, Mohammed, S, Hodgson, S V, Chaudary, M A, Fentiman, I S, Ponder, B A, Eeles, R A
Médium: Artigo
Jazyk:Inglês
Vydáno: 1994
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Research Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC1049923/
https://ncbi.nlm.nih.gov/pubmed/8071972
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