Literature DB >> 4064360

X inactivation patterns in two syndromes with probable X-linked dominant, male lethal inheritance.

P Wieacker, J Zimmer, H H Ropers.   

Abstract

For Incontinentia pigmenti Bloch-Sulzberger (IP) and Aicardi syndrome, an X-linked dominant transmission with lethality in hemizygous males has been proposed. The typical transition from inflammation to verrucous hypertrophy and hyperpigmented skin areas in IP suggests a gradual replacement of defective cells by normal cells. This would imply a preferential inactivation of the X chromosome carrying the IP gene with a proliferative advantage of this cell population. We have confirmed this hypothesis by demonstrating that the same X chromosome is preferentially active in fibroblasts grown from normal and hyperpigmented skin of an affected girl. In contrast, X inactivation was random in a girl with Aicardi syndrome.

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Year:  1985        PMID: 4064360     DOI: 10.1111/j.1399-0004.1985.tb00392.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  13 in total

1.  Monozygotic twins discordant for Aicardi syndrome.

Authors:  T Costa; W Greer; G Rysiecki; J R Buncic; P N Ray
Journal:  J Med Genet       Date:  1997-08       Impact factor: 6.318

Review 2.  30 Years of NF-κB: A Blossoming of Relevance to Human Pathobiology.

Authors:  Qian Zhang; Michael J Lenardo; David Baltimore
Journal:  Cell       Date:  2017-01-12       Impact factor: 41.582

3.  Selection against lethal alleles in females heterozygous for incontinentia pigmenti.

Authors:  B R Migeon; J Axelman; S Jan de Beur; D Valle; G A Mitchell; K N Rosenbaum
Journal:  Am J Hum Genet       Date:  1989-01       Impact factor: 11.025

4.  Carrier detection in X-linked severe combined immunodeficiency based on patterns of X chromosome inactivation.

Authors:  J M Puck; R L Nussbaum; M E Conley
Journal:  J Clin Invest       Date:  1987-05       Impact factor: 14.808

Review 5.  Incontinentia pigmenti (Bloch-Sulzberger syndrome).

Authors:  S J Landy; D Donnai
Journal:  J Med Genet       Date:  1993-01       Impact factor: 6.318

6.  Novel corneal features in two males with incontinentia pigmenti.

Authors:  E J Mayer; G N Shuttleworth; K L Greenhalgh; J E Sansom; R H B Grey; S Kenwrick
Journal:  Br J Ophthalmol       Date:  2003-05       Impact factor: 4.638

7.  Incontinentia pigmenti in a boy with Klinefelter's syndrome.

Authors:  A D Ormerod; M I White; E McKay; A W Johnston
Journal:  J Med Genet       Date:  1987-07       Impact factor: 6.318

8.  Interaction of incontinentia pigmenti and factor VIII mutations in a female with biased X inactivation, resulting in haemophilia.

Authors:  R Coleman; S A Genet; J I Harper; A O Wilkie
Journal:  J Med Genet       Date:  1993-06       Impact factor: 6.318

9.  Renal disease in carrier female dogs with X-linked hereditary nephritis. Implications for female patients with this disease.

Authors:  R Baumal; P Thorner; V E Valli; R McInnes; P Marrano; R Jacobs; A Binnington; A G Bloedow
Journal:  Am J Pathol       Date:  1991-10       Impact factor: 4.307

10.  Non-random X chromosome inactivation in Aicardi syndrome.

Authors:  Tanya N Eble; V Reid Sutton; Haleh Sangi-Haghpeykar; Xiaoling Wang; Weihong Jin; Richard A Lewis; Ping Fang; Ignatia B Van den Veyver
Journal:  Hum Genet       Date:  2009-01-01       Impact factor: 4.132

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