Literature DB >> 16351601

Cytogenetic findings at Down syndrome and their correlation with clinical findings.

Amra Catović1, Sulejman Kendić.   

Abstract

Down syndrome is a genetic state characterized by trisomy of chromosome 21. In the retrospective study for 12 years period (1991-2002) we have conducted correlation between cytogenetics analyses and clinical findings in our centre at 96 male and 83 female patients. Down syndrome was confirmed by cytogenetics analyses in 84 (87.5%) male patients and excluded in 12 (12.5%) male patients. Down syndrome was confirmed by cytogenetics analyses in 71 (85.5%) female patients and excluded in 12 (14.5%) female patients. Most common karyotype is free trisomy found in 139 (89.7%) examinees, than follows translocation form determined in 9 (5.8%), and mosaicism determined in 7 (4.5%) examinees. Our results indicate that cytogenetics analyses are necessary to confirm diagnosis of Down syndrome.

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Year:  2005        PMID: 16351601      PMCID: PMC7202175          DOI: 10.17305/bjbms.2005.3236

Source DB:  PubMed          Journal:  Bosn J Basic Med Sci        ISSN: 1512-8601            Impact factor:   3.363


  9 in total

Review 1.  Familial MCA/MR syndrome due to inherited submicroscopic translocation t(18;21)(q22.1q21.3) with breakpoint at the Down syndrome critical region.

Authors:  Denise Horn; Heidemarie Neitzel; Holger Tönnies; Vera Kalscheuer; Jürgen Kunze; Georg Klaus Hinkel; Oliver Bartsch
Journal:  Am J Med Genet A       Date:  2003-03-15       Impact factor: 2.802

2.  The somatic chromosomes in mongolism.

Authors:  P A JACOBS; A G BAIKIE; W M COURT BROWN; J A STRONG
Journal:  Lancet       Date:  1959-04-04       Impact factor: 79.321

3.  21-trisomy/normal mosaicism in an intelligent child with some mongoloid characters.

Authors:  C M CLARKE; J H EDWARDS; V SMALLPEICE
Journal:  Lancet       Date:  1961-05-13       Impact factor: 79.321

4.  A Mongol girl with 46 chromosomes.

Authors:  P E POLANI; J H BRIGGS; C E FORD; C M CLARKE; J M BERG
Journal:  Lancet       Date:  1960-04-02       Impact factor: 79.321

5.  Down syndrome with pure partial trisomy 21q22 due to a paternal insertion (4;21) uncovered by uncultured amniotic fluid interphase FISH.

Authors:  J Lee; J R Stanley; S A Vaz; J J Mulvihill; P Wilson; D Hopcus-Niccum; Shibo Li
Journal:  Am J Med Genet A       Date:  2005-01-15       Impact factor: 2.802

6.  Can cognitive deterioration associated with Down syndrome be reduced?

Authors:  R Thiel; S W Fowkes
Journal:  Med Hypotheses       Date:  2005       Impact factor: 1.538

Review 7.  A case of myelodysplastic syndrome with acquired monosomy 7 in a child with a constitutional t(1;19) and a mosaicism for trisomy 21.

Authors:  Jie Hu; Sofia Shekhter-Levin; Peter H Shaw; Carolyn Bay; Sally Kochmar; Urvashi Surti
Journal:  Cancer Genet Cytogenet       Date:  2005-01-01

Review 8.  A pediatric approach to the WHO classification of myelodysplastic and myeloproliferative diseases.

Authors:  H Hasle; C M Niemeyer; J M Chessells; I Baumann; J M Bennett; G Kerndrup; D R Head
Journal:  Leukemia       Date:  2003-02       Impact factor: 11.528

Review 9.  Fetal and neonatal leukemia.

Authors:  Hart Isaacs
Journal:  J Pediatr Hematol Oncol       Date:  2003-05       Impact factor: 1.289

  9 in total

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