Literature DB >> 8728687

Hypomelanosis of Ito and X;autosome translocations: a unifying hypothesis.

E Hatchwell1.   

Abstract

Hypomelanosis of Ito is a sporadic multisystem disorder known to be associated in many cases with chromosomal mosaicism. While no particular pattern is generally evident for the specific chromosomes involved in such patients, a subgroup of female patients exists in whom the common factor is the presence of a balanced, constitutional X;autosome translocation, with a cytogenetic breakpoint in the pericentromeric region of the X. It is argued here that the phenotype in these cases results not from the interruption of X linked genes but from the presence of mosaic functional disomy of X sequences above the breakpoint.

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Year:  1996        PMID: 8728687      PMCID: PMC1051863          DOI: 10.1136/jmg.33.3.177

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  47 in total

1.  Isolation of a candidate gene for Menkes disease that encodes a potential heavy metal binding protein.

Authors:  J Chelly; Z Tümer; T Tønnesen; A Petterson; Y Ishikawa-Brush; N Tommerup; N Horn; A P Monaco
Journal:  Nat Genet       Date:  1993-01       Impact factor: 38.330

2.  Three patients with ring (X) chromosomes and a severe phenotype.

Authors:  N R Dennis; A L Collins; J A Crolla; A E Cockwell; A M Fisher; P A Jacobs
Journal:  J Med Genet       Date:  1993-06       Impact factor: 6.318

Review 3.  Incontinentia pigmenti nomenclature.

Authors:  V P Sybert
Journal:  Am J Hum Genet       Date:  1994-07       Impact factor: 11.025

4.  45,X/46,X,+r(X) can have a distinct phenotype different from Ullrich-Turner syndrome.

Authors:  M Grompe; N Rao; F F Elder; C T Caskey; F Greenberg
Journal:  Am J Med Genet       Date:  1992-01-01

5.  Molecular cytogenetic analysis of a duplication Xp in a male: further delineation of a possible sex influencing region on the X chromosome.

Authors:  P N Rao; K Klinepeter; W Stewart; R Hayworth; R Grubs; M J Pettenati
Journal:  Hum Genet       Date:  1994-08       Impact factor: 4.132

Review 6.  Small marker X chromosomes lack the X inactivation center: implications for karyotype/phenotype correlations.

Authors:  D J Wolff; C J Brown; S Schwartz; A M Duncan; U Surti; H F Willard
Journal:  Am J Hum Genet       Date:  1994-07       Impact factor: 11.025

7.  A male with two contiguous inactivation centers on a single X chromosome: study of X inactivation and XIST expression.

Authors:  F Muscatelli; D Lena; M G Mettei; M Fontes
Journal:  Hum Mol Genet       Date:  1992-05       Impact factor: 6.150

8.  Deficient transcription of XIST from tiny ring X chromosomes in females with severe phenotypes.

Authors:  B R Migeon; S Luo; B A Stasiowski; M Jani; J Axelman; D L Van Dyke; L Weiss; P A Jacobs; T L Yang-Feng; J E Wiley
Journal:  Proc Natl Acad Sci U S A       Date:  1993-12-15       Impact factor: 11.205

Review 9.  Proteus syndrome: clinical evidence for somatic mosaicism and selective review.

Authors:  M M Cohen
Journal:  Am J Med Genet       Date:  1993-10-01

10.  The gene for the familial form of incontinentia pigmenti (IP2) maps to the distal part of Xq28.

Authors:  A Smahi; C Hyden-Granskog; B Peterlin; P Vabres; S Heuertz; M C Fulchignoni-Lataud; N Dahl; P Labrune; B Le Marec; C Piussan
Journal:  Hum Mol Genet       Date:  1994-02       Impact factor: 6.150

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  5 in total

1.  DNA methylation analysis of a de novo balanced X;13 translocation in a girl with abnormal phenotype: evidence for functional duplication of the whole short arm of the X chromosome.

Authors:  A Myszka; P Karpinski; I Makowska; M Lassota; B Przelozna; R Slezak; M M Sasiadek
Journal:  J Appl Genet       Date:  2010       Impact factor: 3.240

Review 2.  Genetic control of X inactivation and processes leading to X-inactivation skewing.

Authors:  J W Belmont
Journal:  Am J Hum Genet       Date:  1996-06       Impact factor: 11.025

3.  The neurologic aspects of hypomelanosis of Ito: Case report and review of the literature.

Authors:  Amal Y Kentab; Hamdy H Hassan; Muddathir H A Hamad; Ahmed Alhumidi
Journal:  Sudan J Paediatr       Date:  2014

4.  An unbalanced submicroscopic translocation t(8;16)(q24.3;p13.3)pat associated with tuberous sclerosis complex, adult polycystic kidney disease, and hypomelanosis of Ito.

Authors:  B H Eussen; G Bartalini; L Bakker; P Balestri; C Di Lucca; J O Van Hemel; H Dauwerse; A M van Den Ouweland; C Ris-Stalpers; S Verhoef; D J Halley; A Fois
Journal:  J Med Genet       Date:  2000-04       Impact factor: 6.318

5.  Total Hemi-overgrowth in Pigmentary Mosaicism of the (Hypomelanosis of) Ito Type: Eight Case Reports.

Authors:  Vito Pavone; Salvatore Santo Signorelli; Andrea Domenico Praticò; Giovanni Corsello; Salvatore Savasta; Raffaele Falsaperla; Piero Pavone; Giuseppe Sessa; Martino Ruggieri
Journal:  Medicine (Baltimore)       Date:  2016-03       Impact factor: 1.889

  5 in total

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