Literature DB >> 15614723

Cytogenetics of genetic counseling patients in Pelotas, Rio Grande do Sul, Brazil.

A C Duarte1, E Cunha, J M Roth, F L S Ferreira, G L Garcias, M G Martino-Roth.   

Abstract

From 1986 to 2002, we examined the chromosomal composition of 916 patients attended by two genetic counseling services in the city of Pelotas, in the Brazilian State of Rio Grande do Sul, to determine the genetic causes of their disturbances. Patterns of G-banding using trypsin and Giemsa (GTG) and C-banding using barium and Giemsa (CBG) were studied using phytohemagglutinin M-stimulated lymphocytes cultured from peripheral blood. Among the patients, 110 had Down's syndrome, 7 had Edward's syndrome, 4 had Patau's syndrome, 29 had Turner's syndrome, 5 had Klinefelter's syndrome, and 3 had "cri-du-chat" syndrome. Abnormal chromosomes were observed in 29.3% of the patients. Most of these (56.3%) were numerical abnormalities, with the remaining being structural variants.

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Year:  2004        PMID: 15614723

Source DB:  PubMed          Journal:  Genet Mol Res        ISSN: 1676-5680


  14 in total

1.  Cytogenetic analysis of chromosomal abnormalities in Sri Lankan children.

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2.  Longevity and Patau syndrome: what determines survival?

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3.  Cytogenetic Analysis for Suspected Chromosomal Abnormalities; A Five Years Experience.

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Journal:  J Clin Diagn Res       Date:  2016-09-01

4.  Cytogenetic status of patients with congenital malformations or suspected chromosomal abnormalities in Turkey: a comprehensive cytogenetic survey of 11,420 patients.

Authors:  Osman Demirhan; Erdal Tunç
Journal:  Chromosoma       Date:  2022-10-11       Impact factor: 2.919

5.  Three Offspring with Cri-du-Chat Syndrome from Phenotypically Normal Parents.

Authors:  Dilek U Alkaya; Birsen Karaman; Beyhan Tüysüz
Journal:  Mol Syndromol       Date:  2020-04-02

6.  Cytogenetic Studies of Rwandan Pediatric Patients Presenting with Global Developmental Delay, Intellectual Disability and/or Multiple Congenital Anomalies.

Authors:  Annette Uwineza; Janvier Hitayezu; Mauricette Jamar; Jean-Hubert Caberg; Seraphine Murorunkwere; Ndinkabandi Janvier; Vincent Bours; Leon Mutesa
Journal:  J Trop Pediatr       Date:  2015-10-27       Impact factor: 1.165

7.  Pattern of chromosomal aberrations in patients from north East iran.

Authors:  Saeedeh Ghazaey; Farzaneh Mirzaei; Mitra Ahadian; Fatemeh Keifi; Tootian Semiramis; Mohammad Reza Abbaszadegan
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8.  [The Cri du Chat syndrome: report of an observation].

Authors:  Karim Ouldim; Imane Samri; Laila Bouguenouch; Hasna Hamdaoui; Ihsan El Otmani; Mohamed Hbibi; Sana Chaouki; Moustapha Hida
Journal:  Pan Afr Med J       Date:  2012-01-12

Review 9.  Cri du Chat syndrome.

Authors:  Paola Cerruti Mainardi
Journal:  Orphanet J Rare Dis       Date:  2006-09-05       Impact factor: 4.123

10.  Sex chromosome aneuploidy in cytogenetic findings of referral patients from south of Iran.

Authors:  Najmeh Jouyan; Elham Davoudi Dehaghani; Sara Senemar; Ashraf Shojaee; Hossein Mozdarani
Journal:  Iran J Reprod Med       Date:  2012-03
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