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網膜母細胞腫에 對하여

Retinoblastoma

대한안과학회지 1970년 11권 4호 p.59 ~ 65
韓洪株 (  ) - 全南大學校 醫科大學 眼科學敎室

朴秉日 (  ) - 全南大學校 醫科大學 眼科學敎室

Abstract


Retinoblastoma has been established as an inheritable disease. To the development of sporadic cases the mutation can be ascribable. Once the gene has been established, however, it is transmitted as; an autosomal dominant characteristics with incomplete penetrance. The cases reported here was established in siblings which are of the extremely rare entities. Two families are reported here, which is one of the rare occurrence.
1st. Family:
The retinoblastoma affect 4 siblings(male, 2. female, 2) in 8 siblings(male, 3. female, 5). Of this 4 cases, 3 died of progression of retinoblastoma, while the one left was in apparent. good health with early enucleation.
2nd. family:
Retinoblastoma existed in all two siblings(male, 1. female, 1). The male dead 1 year after diagnosis of retinoblastoma and the other one refused radical treatment -and lost in follow up.

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