Literature DB >> 19701220

Supernumerary marker chromosome 15 in a male with azoospermia and open bite deformity.

Altuğ Koç1, S Odül Onur, Mehmet Ali Ergün, E Ferda Perçin.   

Abstract

Supernumerary marker chromosome 15 (sSMC[15]) is the most frequent marker chromosome, and it is generally regarded as unimportant if it does not contain the Prader-Willi/Angelman syndrome critical region (PWACR). The clinical importance of the larger markers in association with the critical region is mentioned in almost all reports related to marker chromosome 15, and smaller markers are solely associated with minor dysmorphic features, azoospermia and recurrent miscarriages. However, these small sSMC(15)s without the PWACR may also determine a specific phenotype. A dysmorphic examination of an azoospermic patient in a genetics clinic was performed and was followed by a peripheral blood lymphocyte chromosomal analysis according to standard cytogenetic methods. Nucleolar region (NOR) banding, C-banding, fluorescence in situ hybridization and a molecular investigation of Y-microdeletions were also performed. The clinical evaluation identified dysmorphic features accompanied with azoospermia and severe 'Angle Class II, Division 1 Open Bite Deformity'. The molecular cytogenetic study revealed the small sSMC(15). In addition, a Y-microdeletion analysis showed that the azoospermia was not the result of a deletion. Although the presented case might represent a coincidental example of supernumerary marker 15 and mandibular anomaly association, the condition may also define a specific phenotype that may be more than azoospermia. This condition may be characterized by infertility, malar hypoplasia, mandibular anomaly, keloid formation and minor dysmorphic features.

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Year:  2009        PMID: 19701220      PMCID: PMC3735005          DOI: 10.1038/aja.2009.37

Source DB:  PubMed          Journal:  Asian J Androl        ISSN: 1008-682X            Impact factor:   3.285


  21 in total

1.  Supernumerary marker 15 chromosome in a patient with Prader-Willi syndrome.

Authors:  D Borelina; S Esperante; V Gutnisky; V Ferreiro; M Ferrer; F Giliberto; G Frechtel; L Francipane; I Szijan
Journal:  Clin Genet       Date:  2004-03       Impact factor: 4.438

Review 2.  Prenatal diagnosis of supernumerary marker 15 chromosomes and exclusion of uniparental disomy for chromosome 15.

Authors:  P D Cotter; C T Ledesma; L G Dietz; S Pusso; M M Wohlferd; J D Goldberg
Journal:  Prenat Diagn       Date:  1999-08       Impact factor: 3.050

Review 3.  Marker chromosomes in fetal loss.

Authors:  C Kumar; S M Kleyman; R V Samonte; R S Verma
Journal:  Hum Reprod       Date:  1997-06       Impact factor: 6.918

4.  Characterization of a small supernumerary ring X chromosome by fluorescence in situ hybridization.

Authors:  A M Duncan; A Macdonald; C J Brown; D Wolff; H F Willard; B Sutton
Journal:  Am J Med Genet       Date:  1993-12-01

Review 5.  Prader-Willi syndrome with a karyotype 47,XY,+min(15)(pter->q11.1:) and maternal UPD 15--case report plus review of similar cases.

Authors:  Thomas Liehr; Elke Brude; Gabriele Gillessen-Kaesbach; Rainer König; Kristin Mrasek; Ferdinand von Eggeling; Heike Starke
Journal:  Eur J Med Genet       Date:  2005-02-17       Impact factor: 2.708

Review 6.  The inv dup(15) or idic(15) syndrome: a clinically recognisable neurogenetic disorder.

Authors:  Agatino Battaglia
Journal:  Brain Dev       Date:  2005-04-22       Impact factor: 1.961

Review 7.  Ring chromosome X in a child with manifestations of Kabuki syndrome.

Authors:  M J McGinniss; D H Brown; L W Burke; J T Mascarello; M C Jones
Journal:  Am J Med Genet       Date:  1997-05-02

8.  Supernumerary tricentric derivative chromosome 15 in two boys with intractable epilepsy: another mechanism for partial hexasomy.

Authors:  S M Mann; N J Wang; D H Liu; L Wang; R A Schultz; N Dorrani; M Sigman; N C Schanen
Journal:  Hum Genet       Date:  2004-05-13       Impact factor: 4.132

9.  Cytogenetic and molecular characterization of inverted duplicated chromosomes 15 from 11 patients.

Authors:  S D Cheng; N B Spinner; E H Zackai; J H Knoll
Journal:  Am J Hum Genet       Date:  1994-10       Impact factor: 11.025

10.  Autistic symptoms among children and young adults with isodicentric chromosome 15.

Authors:  S Rineer; B Finucane; E W Simon
Journal:  Am J Med Genet       Date:  1998-09-07
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  5 in total

1.  Decreased XY recombination and disturbed meiotic prophase I progression in an infertile 48, XYY, +sSMC man.

Authors:  Liu Wang; Zhipeng Xu; Furhan Iqbal; Liangwen Zhong; Yuanwei Zhang; Caiyun Wu; Guixiang Zhou; Hanwei Jiang; Ihtisham Bukhari; Howard J Cooke; Qinghua Shi
Journal:  Chromosome Res       Date:  2015-01-28       Impact factor: 5.239

2.  Male Infertility Associated with a Supernumerary Marker Chromosome.

Authors:  Seung Hun Song; Sang Hee Park; Eunah Shin; Jae Hung Jung; Sung Han Shim; Dong Suk Kim
Journal:  World J Mens Health       Date:  2017-09-06       Impact factor: 5.400

3.  Genetic dosage and position effect of small supernumerary marker chromosome (sSMC) in human sperm nuclei in infertile male patient.

Authors:  Marta Olszewska; Elzbieta Wanowska; Archana Kishore; Nataliya Huleyuk; Andrew P Georgiadis; Alexander N Yatsenko; Mariya Mikula; Danuta Zastavna; Ewa Wiland; Maciej Kurpisz
Journal:  Sci Rep       Date:  2015-11-30       Impact factor: 4.379

4.  Prenatal diagnosis and genetic counseling in a fetus associated with risk of Angelman syndrome with a small supernumerary marker chromosome derived from chromosome 22.

Authors:  Yu-An Hu; Yingxia Cui; Xiaobo Fan; Qiuyue Wu; Weiwei Li; Weiping Wang
Journal:  Mol Cytogenet       Date:  2016-05-03       Impact factor: 2.009

Review 5.  Molecular Characterization of Mosaicism for a Small Supernumerary Marker Chromosome Derived from Chromosome Y in an Infertile Male with Apparently Normal Phenotype: A Case Report and Literature Review.

Authors:  Na An; Yang Yu; Qi Xi; Fagui Yue; Ruizhi Liu; Shibo Li; Ruixue Wang
Journal:  Biomed Res Int       Date:  2019-11-19       Impact factor: 3.411

  5 in total

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