Literature DB >> 3177451

A new syndrome with mental retardation, short stature and an Xq duplication.

A Thode1, M W Partington, M Y Yip, C Chapman, V F Richardson, G Turner.   

Abstract

We describe a new X-linked syndrome of marked short stature, severe intellectual handicap and an unusual facial appearance. High resolution prometaphase banding showed affected males to have an X chromosome tandem duplication; their karyotypes were designated 46,dup(X) (q13.1-q21.1)Y. In carrier females the abnormal X chromosome was late replicating. To verify the duplication, gene dosage studies were performed using an enzyme assay and DNA techniques. Prenatal diagnosis is available for carrier females using chromosome analysis of amniocytes or chorionic villi.

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Year:  1988        PMID: 3177451     DOI: 10.1002/ajmg.1320300125

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  16 in total

1.  Duplications of the X chromosome in males: evidence that most parts of the X chromosome can be active in two copies.

Authors:  M Schmidt; D Du Sart; P Kalitsis; M Leversha; S Dale; L Sheffield; D Toniolo
Journal:  Hum Genet       Date:  1991-03       Impact factor: 4.132

2.  Physical mapping of an Xq-proximal interstitial duplication in a male.

Authors:  F Muscatelli; J M Verna; N Philip; A Moncla; M G Mattei; J F Mattei; M Fontes
Journal:  Hum Genet       Date:  1992-03       Impact factor: 4.132

3.  Sex reversal in a child with a 46,X,Yp+ karyotype: support for the existence of a gene(s), located in distal Xp, involved in testis formation.

Authors:  T Ogata; J R Hawkins; A Taylor; N Matsuo; J Hata; P N Goodfellow
Journal:  J Med Genet       Date:  1992-04       Impact factor: 6.318

Review 4.  Hypomelanosis of Ito and X;autosome translocations: a unifying hypothesis.

Authors:  E Hatchwell
Journal:  J Med Genet       Date:  1996-03       Impact factor: 6.318

5.  Familial skewed X inactivation: a molecular trait associated with high spontaneous-abortion rate maps to Xq28.

Authors:  E Pegoraro; J Whitaker; P Mowery-Rushton; U Surti; M Lanasa; E P Hoffman
Journal:  Am J Hum Genet       Date:  1997-07       Impact factor: 11.025

6.  An apparent excess of sex- and reproduction-related genes on the human X chromosome.

Authors:  G M Saifi; H S Chandra
Journal:  Proc Biol Sci       Date:  1999-01-22       Impact factor: 5.349

7.  A familial Xp+ chromosome, dup (Xq26.3-->qter).

Authors:  A I Vasquez; H Rivera; L Bobadilla; J A Crolla
Journal:  J Med Genet       Date:  1995-11       Impact factor: 6.318

8.  The Juberg-Marsidi syndrome maps to the proximal long arm of the X chromosome (Xq12-q21).

Authors:  P Saugier-Veber; V Abadie; A Moncla; M Mathieu; C Piussan; C Turleau; J F Mattei; A Munnich; S Lyonnet
Journal:  Am J Hum Genet       Date:  1993-06       Impact factor: 11.025

9.  Familial interstitial Xq27.3q28 duplication encompassing the FMR1 gene but not the MECP2 gene causes a new syndromic mental retardation condition.

Authors:  Marlène Rio; Valérie Malan; Sarah Boissel; Annick Toutain; Ghislaine Royer; Stéphanie Gobin; Nicole Morichon-Delvallez; Catherine Turleau; Jean-Paul Bonnefont; Arnold Munnich; Michel Vekemans; Laurence Colleaux
Journal:  Eur J Hum Genet       Date:  2009-10-21       Impact factor: 4.246

10.  Subterminal deletion/duplication event in an affected male due to maternal X chromosome pericentric inversion.

Authors:  Nadja Kokalj-Vokac; Natasa Marcun-Varda; Andreja Zagorac; Alenka Erjavec-Skerget; Boris Zagradisnik; Mirjana Todorovic; Alojz Gregoric
Journal:  Eur J Pediatr       Date:  2004-08-12       Impact factor: 3.183

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