The ophthalmological significance of the basal cell naevus syndrome.

Australian journal of ophthalmology Pub Date : 1983-11-01
P A Rogers
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Abstract

Ten cases of the basal cell naevus syndrome (BCNS) are reported. The study is based on clinical findings with no investigations beyond two skull radiographs. The diagnosis is made on some or all of the following findings: family history, jaw cysts, progressive development of basal cell carcinomas (BCCs), pitting of the palms and soles, frontal bossing, abnormality of the skeletal system and ectopic calcification. Eight of the cases are in one family covering three generations. With the exception of a one-year-old child in the third generation (not included) all of this group have the syndrome. The dominant trait is demonstrated, as is the high degree of expressivity and penetrance. Genetic counselling is essential where applicable. Sympathetic regular clinical examination over a lifetime is recommended to avoid disastrous complications.

基底细胞痣综合征的眼科学意义。
本文报告基底细胞痣综合征(BCNS) 10例。该研究基于临床发现,除了两次颅骨x线片外没有任何调查。诊断依据如下部分或全部表现:家族史、颌骨囊肿、基底细胞癌(BCCs)的进展、手掌和脚底凹陷、额部隆起、骨骼系统异常和异位钙化。其中8个病例来自一个家庭,涵盖三代人。除了第三代的一个一岁的孩子(不包括在内),所有这些人都有这种综合症。显性性状被证明,因为是高度的表达和外显率。遗传咨询在适用的情况下是必不可少的。建议终生定期临床检查交感神经系统,以避免灾难性的并发症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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