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分子研究在色素失禁症患者中的应用。

Utility of molecular studies in incontinentia pigmenti patients.

机构信息

Department of Genetic Medicine, Sir Ganga Ram Hospital, New Delhi, India.

出版信息

Indian J Med Res. 2011 Apr;133(4):442-5.

Abstract

The diagnosis of incontinentia pigmenti (IP) is fairly easy in the presence of classical features, but can be difficult in cases with partial or non-classical features, especially in the parents. The demonstration that the disease is caused by mutations in the NEMO gene, has remarkably improved genetic counselling for this disorder. We present four families of IP in whom molecular studies established an unequivocal diagnosis in the affected daughters, and showed two mothers to be carriers, thus allowing accurate genetic counselling and prenatal diagnosis.

摘要

色素失禁症(IP)的诊断在具有典型特征时相当容易,但在具有部分或非典型特征的情况下可能较为困难,尤其是在父母中。证明该疾病是由 NEMO 基因突变引起的,极大地改善了对此类疾病的遗传咨询。我们介绍了四个 IP 家族,在这些家族中,分子研究在受影响的女儿中确立了明确的诊断,并显示出两名母亲是携带者,从而可以进行准确的遗传咨询和产前诊断。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4db8/3103180/140f37c4c51e/IJMR-133-442-g001.jpg

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