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神经纤维瘤病:一种具有两个严重问题高发年龄段的肿瘤性出生缺陷。

Neurofibromatosis: a neoplastic birth defect with two age peaks of severe problems.

作者信息

Riccardi V M, Kleiner B

出版信息

Birth Defects Orig Artic Ser. 1977;13(3C):131-8.

PMID:407957
Abstract

A survey involving more than 400,000 patient sources revealed a population of 129 NFT patients relatively unbiased by the specific character of the disease (eg neurologic vs orthopedic problems), though biased in terms of severity. Two age peaks of severe disease were demononstrated, one early in life (10 yr or less) and one late (apex in 36- to 50-yr group). Neural crest-derived malignancies were the critical component of the second peak (75% of severe cases). The high burden nature of the disorder is emphasized by the fact that moderate and severe cases amounted to 64% in the survey population (ie those brought to medical attention) and 26% in nonproband affected family members in 46 families. In addition, even correcting for 5% of ascertainment of minimal-mild cases and 61% ascertainment of moderate-sever cases, 7% of the presumed NFT population may be considereed at risk for severe problems.

摘要

一项涉及超过400,000个患者来源的调查显示,有129名NFT患者群体,相对不受疾病特定特征(如神经与骨科问题)的影响,尽管在严重程度方面存在偏差。显示出严重疾病的两个年龄高峰,一个在生命早期(10岁或更小),一个在晚期(在36至50岁组达到顶峰)。神经嵴衍生的恶性肿瘤是第二个高峰的关键组成部分(75%的严重病例)。该疾病的高负担性质通过以下事实得到强调:在调查人群(即那些引起医疗关注的人群)中,中度和重度病例占64%,在46个家庭的非先证者受影响家庭成员中占26%。此外,即使校正5%的轻度至轻度病例确诊率和61%的中度至重度病例确诊率,假定的NFT人群中仍有7%可能被认为有发生严重问题的风险。

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