Literature DB >> 19116729

Non-random X chromosome inactivation in Aicardi syndrome.

Tanya N Eble1, V Reid Sutton, Haleh Sangi-Haghpeykar, Xiaoling Wang, Weihong Jin, Richard A Lewis, Ping Fang, Ignatia B Van den Veyver.   

Abstract

Most females have random X-chromosome inactivation (XCI), defined as an equal likelihood for inactivation of the maternally- or paternally-derived X chromosome in each cell. Several X-linked disorders have been associated with a higher prevalence of non-random XCI patterns, but previous studies on XCI patterns in Aicardi syndrome were limited by small numbers and older methodologies, and have yielded conflicting results. We studied XCI patterns in DNA extracted from peripheral blood leukocytes of 35 girls with typical Aicardi syndrome (AIC) from 0.25 to 16.42 years of age, using the human androgen receptor assay. Data on 33 informative samples showed non-random XCI in 11 (33%), defined as a >80:20% skewed ratio of one versus the other X chromosome being active. In six (18%) of these, there was a >95:5% extremely skewed ratio of one versus the other X chromosome being active. XCI patterns on maternal samples were not excessively skewed. The prevalence of non-random XCI in Aicardi syndrome is significantly different from that in the general population (p < 0.0001) and provides additional support for the hypothesis that Aicardi syndrome is an X-linked disorder. We also investigated the correlation between X-inactivation patterns and clinical severity and found that non-random XCI is associated with a high neurological composite severity score. Conversely, a statistically significant association was found between random XCI and the skeletal composite score. Correlations between X-inactivation patterns and individual features were made and we found a significant association between vertebral anomalies and random XCI.

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Year:  2009        PMID: 19116729      PMCID: PMC2660246          DOI: 10.1007/s00439-008-0615-4

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  33 in total

1.  Aicardi's syndrome in a male child: an unusual presentation.

Authors:  K C Aggarwal; A Aggarwal; M S Prasad; R N Salhan; A Upadhaya
Journal:  Indian Pediatr       Date:  2000-05       Impact factor: 1.411

2.  The dynamics of X-inactivation skewing as women age.

Authors:  C Hatakeyama; C L Anderson; C L Beever; M S Peñaherrera; C J Brown; W P Robinson
Journal:  Clin Genet       Date:  2004-10       Impact factor: 4.438

3.  X inactivation in females with X-linked disease.

Authors:  J M Puck; H F Willard
Journal:  N Engl J Med       Date:  1998-01-29       Impact factor: 91.245

4.  Evidence that skewed X inactivation is not needed for the phenotypic expression of Aicardi syndrome.

Authors:  H M Hoag; S A Taylor; A M Duncan; M M Khalifa
Journal:  Hum Genet       Date:  1997-09       Impact factor: 4.132

5.  EEG recognition of Aicardi's syndrome.

Authors:  R G Fariello; R W Chun; J M Doro; J R Buncic; J S Prichard
Journal:  Arch Neurol       Date:  1977-09

6.  Aicardi syndrome in a male infant.

Authors:  P Curatolo; G Libutti; B Dallapiccola
Journal:  J Pediatr       Date:  1980-02       Impact factor: 4.406

Review 7.  Aicardi syndrome.

Authors:  Jean Aicardi
Journal:  Brain Dev       Date:  2005-04       Impact factor: 1.961

8.  Skewed X-chromosome inactivation is a common feature of X-linked mental retardation disorders.

Authors:  Robert M Plenge; Roger A Stevenson; Herbert A Lubs; Charles E Schwartz; Huntington F Willard
Journal:  Am J Hum Genet       Date:  2002-05-30       Impact factor: 11.025

9.  Microphthalmia with linear skin defects (MLS), Aicardi, and Goltz syndromes: are they related X-linked dominant male-lethal disorders?

Authors:  I B Van den Veyver
Journal:  Cytogenet Genome Res       Date:  2002       Impact factor: 1.636

10.  Aicardi's syndrome: a report of four cases and review of the literature.

Authors:  G T Denslow; R M Robb
Journal:  J Pediatr Ophthalmol Strabismus       Date:  1979 Jan-Feb       Impact factor: 1.402

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  5 in total

1.  Ophthalmologic findings in Aicardi syndrome.

Authors:  Gary Fruhman; Tanya N Eble; Nikki Gambhir; V Reid Sutton; Ignatia B Van den Veyver; Richard A Lewis
Journal:  J AAPOS       Date:  2012-06       Impact factor: 1.220

2.  Laterality of brain and ocular lesions in Aicardi syndrome.

Authors:  Michelle T Cabrera; Bryan J Winn; Travis Porco; Zoe Strominger; A James Barkovich; Creig S Hoyt; Mari Wakahiro; Elliott H Sherr
Journal:  Pediatr Neurol       Date:  2011-09       Impact factor: 3.372

3.  A genome-wide screen for copy number alterations in Aicardi syndrome.

Authors:  Xiaoling Wang; V Reid Sutton; Tanya N Eble; Richard Alan Lewis; Preethi Gunaratne; Ankita Patel; Ignatia B Van den Veyver
Journal:  Am J Med Genet A       Date:  2009-10       Impact factor: 2.802

4.  Independent variant analysis of TEAD1 and OCEL1 in 38 Aicardi syndrome patients.

Authors:  Bibiana K Y Wong; Vernon R Sutton; Richard A Lewis; Ignatia B Van den Veyver
Journal:  Mol Genet Genomic Med       Date:  2017-01-25       Impact factor: 2.183

Review 5.  Genetic heterogeneity in corpus callosum agenesis.

Authors:  Monica-Cristina Pânzaru; Setalia Popa; Ancuta Lupu; Cristina Gavrilovici; Vasile Valeriu Lupu; Eusebiu Vlad Gorduza
Journal:  Front Genet       Date:  2022-09-30       Impact factor: 4.772

  5 in total

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