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一名因X染色体失活偏斜而患丹特病的女性患者。

A female patient with Dent disease due to skewed X-chromosome inactivation.

作者信息

D'Ambrosio Viola, Wan Elizabeth R, Siew Keith, Hayes Wesley, Walsh Stephen B

机构信息

London Tubular Centre, UCL Department of Renal Medicine, University College London, London, UK.

Università Cattolica del Sacro Cuore di Roma, Rome, Italy.

出版信息

Clin Kidney J. 2024 Apr 2;17(6):sfae092. doi: 10.1093/ckj/sfae092. eCollection 2024 Jun.

Abstract

X-linked proximal tubulopathies are rare diseases that predominantly affect men. Women are generally carriers and clinical or biochemical manifestations are usually absent or mild. We present the case of a young woman who presented with a full phenotype of Dent disease type 1 due to a de novo mutation in the gene and a skewed X-chromosome inactivation. Although cases of overt Dent disease type 2 and Lowe syndrome in women have been described in the literature, to our knowledge this is the first case of overt Dent disease type 1.

摘要

X连锁近端肾小管病是一种罕见疾病,主要影响男性。女性通常为携带者,临床或生化表现通常不存在或很轻微。我们报告了一例年轻女性病例,该女性因基因新发突变和X染色体失活偏斜而表现出完全型1型丹特病的表型。尽管文献中已描述了女性显性2型丹特病和洛氏综合征的病例,但据我们所知,这是首例显性1型丹特病病例。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c111/11170036/46e9956f2047/sfae092fig1.jpg

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