Literature DB >> 16100724

Non-skewed X-inactivation may cause mental retardation in a female carrier of X-linked alpha-thalassemia/mental retardation syndrome (ATR-X): X-inactivation study of nine female carriers of ATR-X.

Takahito Wada1, Hideo Sugie, Yoshimitsu Fukushima, Shinji Saitoh.   

Abstract

X-linked alpha-thalassemia/mental retardation syndrome (ATR-X) is a syndromic form of X-linked mental retardation. We investigated the X-inactivation status of nine female ATR-X carriers by methylation-specific PCR of the HUMARA gene. Six carriers demonstrated a skewed X-inactivation pattern (>90:10) and one showed a non-skewed pattern (72:28), while two were uninformative because of homozygosity for the CAG repeat polymorphic alleles in the HUMARA. Only the carrier mother who showed non-skewed X-inactivation had moderate mental retardation. These findings suggest that mutations in ATRX may cause mental retardation in females, if the X chromosome carrying mutated ATRX is not properly inactivated. (c) 2005 Wiley-Liss, Inc.

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Year:  2005        PMID: 16100724     DOI: 10.1002/ajmg.a.30901

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  4 in total

Review 1.  X chromosome inactivation in clinical practice.

Authors:  Karen Helene Orstavik
Journal:  Hum Genet       Date:  2009-04-25       Impact factor: 4.132

2.  The first case of X-linked Alpha-thalassemia/mental retardation (ATR-X) syndrome in Korea.

Authors:  Ki Wook Yun; Soo Ahn Chae; Jung Ju Lee; Sin Weon Yun; Byoung Hoon Yoo; In Seok Lim; Eung Sang Choi; Mi-Kyung Lee
Journal:  J Korean Med Sci       Date:  2010-12-22       Impact factor: 2.153

3.  ATR-X syndrome in two siblings with a novel mutation (c.6718C>T mutation in exon 31).

Authors:  Seema Thakur; Mala Ishrie; Renu Saxena; Sumita Danda; Rose Linda; Auro Viswabandya; I C Verma
Journal:  Indian J Med Res       Date:  2011-10       Impact factor: 2.375

Review 4.  Alpha thalassaemia-mental retardation, X linked.

Authors:  Richard Gibbons
Journal:  Orphanet J Rare Dis       Date:  2006-05-04       Impact factor: 4.123

  4 in total

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