Literature DB >> 7172480

Fertility in patients with X chromosome deletions.

J P Fryns, A Kleczkowska, P Petit, H van den Berghe.   

Abstract

Three fertile, non-mosaic patients with partial monosomy of an X-chromosome (two with Xp deletion with breakpoints at Xp1106 and Xp2101, respectively, and one with a del(Xq25)) were found among 12 females with Xp deletion and three with Xq deletion investigated in this laboratory after the advent of banding techniques. Four phenotypically normal children resulted from a total of seven pregnancies in these women. Three of the children were chromosomally normal and one girl presented the same del(Xp) as her mother. The possibility of having genotypically and phenotypically normal offspring should be taken into account in the management and genetic counseling of children and females with X-chromosome deletions.

Entities:  

Mesh:

Year:  1982        PMID: 7172480     DOI: 10.1111/j.1399-0004.1982.tb01416.x

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


  11 in total

1.  Distal long arm deletions of the X chromosome and ovarian failure.

Authors:  A Bates; P J Howard
Journal:  J Med Genet       Date:  1990-11       Impact factor: 6.318

2.  Short stature in a girl with a terminal Xp deletion distal to DXYS15: localisation of a growth gene(s) in the pseudoautosomal region.

Authors:  T Ogata; P Goodfellow; C Petit; M Aya; N Matsuo
Journal:  J Med Genet       Date:  1992-07       Impact factor: 6.318

3.  An isodicentric X chromosome with short arm fusion in a woman without somatic features of Turner's syndrome.

Authors:  I C Barnes; D J Curtis; S L Duncan
Journal:  J Med Genet       Date:  1987-07       Impact factor: 6.318

4.  Sex chromosome aberrations and stature: deduction of the principal factors involved in the determination of adult height.

Authors:  T Ogata; N Matsuo
Journal:  Hum Genet       Date:  1993-07       Impact factor: 4.132

5.  Deletion (X)(q26.1-->q28) in a proband and her mother: molecular characterization and phenotypic-karyotypic deductions.

Authors:  A T Tharapel; K P Anderson; J L Simpson; P R Martens; R S Wilroy; J C Llerena; C E Schwartz
Journal:  Am J Hum Genet       Date:  1993-03       Impact factor: 11.025

6.  Cytogenetic survey in couples with recurrent fetal wastage.

Authors:  J P Fryns; A Kleczkowska; E Kubień; P Petit; H Van den Berghe
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

7.  Deletion of the short arm of the X chromosome: a hereditary form of Turner syndrome.

Authors:  G Massa; M Vanderschueren-Lodeweyckx; J P Fryns
Journal:  Eur J Pediatr       Date:  1992-12       Impact factor: 3.183

8.  X long-arm deletions. A review of non-mosaic cases studied with banding techniques.

Authors:  L Skibsted; H Westh; E Niebuhr
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

9.  Specific cloning of DNA fragments absent from the DNA of a male patient with an X chromosome deletion.

Authors:  L M Kunkel; A P Monaco; W Middlesworth; H D Ochs; S A Latt
Journal:  Proc Natl Acad Sci U S A       Date:  1985-07       Impact factor: 11.205

10.  The similarity of phenotypic effects caused by Xp and Xq deletions in the human female: a hypothesis.

Authors:  E Therman; B Susman
Journal:  Hum Genet       Date:  1990-07       Impact factor: 4.132

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