Literature DB >> 17113756

Deletion of distal promoter of VCXA in a patient with X-linked ichthyosis associated with borderline mental retardation.

Naoko Hosomi1, Naoki Oiso, Kazuyoshi Fukai, Kazushi Hanada, Hiroko Fujita, Masamitsu Ishii.   

Abstract

BACKGROUND: X-linked ichthyosis (XLI) is caused by deficiency of steroid sulfatase (STS) activity. About 90% XLI patients have large deletions involving the entire STS gene and flanking regions. Recently, VCXA, which is located approximately 0.7Mb telomeric to the STS gene, was reported as a candidate gene for mental retardation (MR) in patients with XLI.
OBJECTIVE: To delineate the X-chromosomal deletion of a XLI patient with borderline mental retardation.
METHODS: We carried out FISH analysis to show that the whole STS gene is deleted, and PCR analysis for fine-scale deletion mapping.
RESULTS: The deleted segment is approximately 1.6Mb in size, and includes the entire STS and VCXB1 genes. VCXA itself is intact, but its promoter is deleted.
CONCLUSION: A deletion that includes the VCXA promoter is associated with borderline mental retardation in a patient with XLI.

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Year:  2006        PMID: 17113756     DOI: 10.1016/j.jdermsci.2006.10.001

Source DB:  PubMed          Journal:  J Dermatol Sci        ISSN: 0923-1811            Impact factor:   4.563


  5 in total

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Authors:  Peter M Elias; Mary L Williams; Eung-Ho Choi; Kenneth R Feingold
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2.  Modulation of neuritogenesis by a protein implicated in X-linked mental retardation.

Authors:  Xinfu Jiao; Hongxin Chen; Jianmin Chen; Karl Herrup; Bonnie L Firestein; Megerditch Kiledjian
Journal:  J Neurosci       Date:  2009-10-07       Impact factor: 6.167

3.  A prenatal diagnosis and genetics study of five pedigrees in the Chinese population with Xp22.31 microduplication.

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Journal:  Mol Cytogenet       Date:  2019-12-11       Impact factor: 2.009

4.  X-linked ichthyosis and Crigler-Najjar syndrome I: Coexistence in a male patient with two copy number variable regions of 2q37.1 and Xp22.3.

Authors:  Jinli Bai; Yujin Qu; Yanyan Cao; Yan Li; Wenhui Zhang; Yuwei Jin; Hong Wang; Fang Song
Journal:  Mol Med Rep       Date:  2015-12-10       Impact factor: 2.952

5.  Comparative Genomic Mapping Implicates LRRK2 for Intellectual Disability and Autism at 12q12, and HDHD1, as Well as PNPLA4, for X-Linked Intellectual Disability at Xp22.31.

Authors:  Jonathan D J Labonne; Terri M Driessen; Marvin E Harris; Il-Keun Kong; Soumia Brakta; John Theisen; Modibo Sangare; Lawrence C Layman; Cheol-Hee Kim; Janghoo Lim; Hyung-Goo Kim
Journal:  J Clin Med       Date:  2020-01-19       Impact factor: 4.241

  5 in total

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