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HLA系统与神经纤维瘤病(冯·雷克林豪森病)。家族研究。

HLA system and neurofibromatosis (von Recklinghausen's disease). Familial studies.

作者信息

Abrahámová J, Majský A, Koutecký J

出版信息

Czech Med. 1985;8(2):68-77.

PMID:3926439
Abstract

The authors performed HLA typing in 18 patients affected by neurofibromatosis (NF) and in 13 of them they also typed all the available members of their families. In 9 families manifesting a kindred occurrence further 16 patients, in whom the disease had not yet been diagnosed, have been unveiled. In 8 families our of nine manifesting a familial load of the disease there was agreement in one HLA haplotype eventually HLA identity among the diseased sibling members. From this point of view it appears that HLA typing in NF might be a valuable contribution especially for the diagnosis of the complete cases in families manifesting a kindred type of NF occurrence. Since NF is a disease perilous through its life endangering complications of a malignant character the authors recommend its dispensation and a concentration of all the NF affected patients and their relatives into a limited number of clinical establishments endowed with a possibility of cooperation with some HLA laboratory.

摘要

作者对18例神经纤维瘤病(NF)患者进行了HLA分型,其中13例还对其所有可及的家庭成员进行了分型。在9个显示家族性发病的家庭中,又发现了16例尚未诊断出该病的患者。在9个显示该病家族聚集性的家庭中,有8个家庭的患病同胞成员之间存在一个HLA单倍型一致,最终出现了HLA相同的情况。从这一点来看,NF的HLA分型可能是一项有价值的贡献,特别是对于诊断显示家族性NF发病类型家庭中的完整病例。由于NF是一种因其危及生命的恶性并发症而危险的疾病,作者建议对其进行分配,并将所有NF患者及其亲属集中到少数具备与某些HLA实验室合作可能性的临床机构中。

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