Literature DB >> 3733078

Ring chromosome 21 in healthy persons: different consequences in females and in males.

B Dallapiccola, V De Filippis, A Notarangelo, G Perla, L Zelante.   

Abstract

A stable ring chromosome 21 was found in an azoospermic man with an otherwise normal phenotype. Meiotic studies in another known azoospermic male with r(21) had indicated that breakdown of spermatogenesis resulted from pairing failure of chromosome 21, followed by degenerative changes in the chromosomes, before the cells had completed the first meiotic division. While primary sterility was a constant feature in the three adult males, eight healthy females with r(21) were fertile. However, they were at risk for Down syndrome and spontaneous abortions.

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Year:  1986        PMID: 3733078     DOI: 10.1007/bf00401230

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


  22 in total

1.  200 infertile males: correlation of chromosome, histological, endocrine and clinical studies.

Authors:  W F Hendry; P E Polani; R C Pugh; I F Sommerville; D M Wallace
Journal:  Br J Urol       Date:  1975

Review 2.  The chromosomal basis of human infertility.

Authors:  A C Chandley
Journal:  Br Med Bull       Date:  1979-05       Impact factor: 4.291

3.  Meiotic studies of translocations causing male sterility in the mouse. I. Autosomal reciprocal translocations.

Authors:  J Forejt; S Gregorová
Journal:  Cytogenet Cell Genet       Date:  1977

4.  Four new cases of ring 21 and 22 including familial transmission of ring 21.

Authors:  C G Palmer; M E Hodes; T Reed; J Kojetin
Journal:  J Med Genet       Date:  1977-02       Impact factor: 6.318

5.  Prenatal detection of an unstable ring 21 chromosome.

Authors:  G Stetten; B Sroka; V L Corson; C D Boehm
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

6.  Ring chromosome 21 in phenotypically apparently normal persons: report of two families from Switzerland and Italy.

Authors:  W Schmid; R Tenconi; C Baccichetti; D Caufin; A Schinzel
Journal:  Am J Med Genet       Date:  1983-11

7.  Ring chromosome 21 in a healthy woman with three spontaneous abortions.

Authors:  K Rhomberg
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

8.  Analysis of banding patterns in a case of ring chromosome 21.

Authors:  C L Richer; N Fitch; S Sitahal; M Murer-Orlando; P Jean
Journal:  Am J Med Genet       Date:  1981

9.  A complex rearrangement involving three autosomes in a phenotypically normal male presenting with sterility.

Authors:  A Joseph; I M Thomas
Journal:  J Med Genet       Date:  1982-10       Impact factor: 6.318

Review 10.  The role of X-chromosome inactivation during spermatogenesis (Drosophila-allocycly-chromosome evolution-male sterility-dosage compensation).

Authors:  E Lifschytz; D L Lindsley
Journal:  Proc Natl Acad Sci U S A       Date:  1972-01       Impact factor: 11.205

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  10 in total

1.  Maternal transmission of ring chromosome 21.

Authors:  I Kennerknecht; G Barbi; W Vogel
Journal:  Hum Genet       Date:  1990-11       Impact factor: 4.132

2.  A case of ring chromosome 15 accompanied by almost normal intelligence.

Authors:  M Kitatani; H Takahashi; M Ozaki; E Okino; T Maruoka
Journal:  Hum Genet       Date:  1990-06       Impact factor: 4.132

3.  Molecular characterisation of partial chromosome 21 aneuploidies by fluorescent PCR.

Authors:  R Valero; G Marfany; R Gil-Benso; M A Ibáñez; I López-Pajares; F Prieto; G Rullan; E Sarret; R Gonzàlez-Duarte
Journal:  J Med Genet       Date:  1999-09       Impact factor: 6.318

Review 4.  Ring chromosomes: from formation to clinical potential.

Authors:  Inna E Pristyazhnyuk; Aleksei G Menzorov
Journal:  Protoplasma       Date:  2017-09-12       Impact factor: 3.356

5.  The normality of sperm in an infertile man with ring chromosome 15: a case report.

Authors:  Kazuyo Nishikawa; Fumiaki Itoi; Miki Nagahara; Mami Jose; Ayumi Matsunaga; Jun Ueda; Takashi Iwamoto
Journal:  J Assist Reprod Genet       Date:  2017-10-23       Impact factor: 3.412

6.  No significant effect of monosomy for distal 21q22.3 on the Down syndrome phenotype in "mirror" duplications of chromosome 21.

Authors:  C Pangalos; D Théophile; P M Sinet; A Marks; D Stamboulieh-Abazis; Z Chettouh; M Prieur; C Verellen; M O Rethoré; J Lejeune
Journal:  Am J Hum Genet       Date:  1992-12       Impact factor: 11.025

Review 7.  Inherited ring chromosomes: an analysis of published cases.

Authors:  G Kosztolányi; K Méhes; E B Hook
Journal:  Hum Genet       Date:  1991-07       Impact factor: 4.132

Review 8.  Two cases of partial trisomy 8p and partial monosomy 21q in a family with a reciprocal translocation (8;21)(p21.1;q22.3).

Authors:  A S Plomp; J J Engelen; J C Albrechts; C E de Die-Smulders; A J Hamers
Journal:  J Med Genet       Date:  1998-07       Impact factor: 6.318

Review 9.  The past, present, and future for constitutional ring chromosomes: A report of the international consortium for human ring chromosomes.

Authors:  Peining Li; Barbara Dupont; Qiping Hu; Marco Crimi; Yiping Shen; Igor Lebedev; Thomas Liehr
Journal:  HGG Adv       Date:  2022-09-10

10.  Meiotic prophase I defects in an oligospermic man with Wolf-Hirschhorn syndrome with ring chromosome 4.

Authors:  Qi Yao; Liu Wang; Bing Yao; Hongliu Gao; Weiwei Li; Xinyi Xia; Qinghua Shi; Yingxia Cui
Journal:  Mol Cytogenet       Date:  2014-07-01       Impact factor: 2.009

  10 in total

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