Identification of Y chromosomal material in turner syndrome by Fluorescence in Situ Hybridisation (FISH)

Turner syndrome is one of the most common chromosomal abnormalities affecting newborn females. More than half of patients with Turner syndrome have a 45X karyotype. The rest of the patients may have structurally abnormal sex chromosomes or are mosaics with normal or abnormal sex chromosomes. Mosa...

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Main Authors: Reena Rahayu Md Zin, Sharifah Noor Akmal, Zubaidah Zakaria, Clarence, Ko Ching Huat, Siti Mariam Yusof, Julia Mohd Idris, Zarina Abdul Latif, Wu, Loo Ling, Wong, Ming
Format: Article
Language:English
Published: Penerbit UKM 2008
Online Access:http://journalarticle.ukm.my/2004/1/Page_22_-_29.pdf
http://journalarticle.ukm.my/2004/
http://www.ppukm.ukm.my/ukmmcjournal/index.php
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Institution: Universiti Kebangsaan Malaysia
Language: English
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spelling my-ukm.journal.20042016-12-14T06:30:38Z http://journalarticle.ukm.my/2004/ Identification of Y chromosomal material in turner syndrome by Fluorescence in Situ Hybridisation (FISH) Reena Rahayu Md Zin, Sharifah Noor Akmal, Zubaidah Zakaria, Clarence, Ko Ching Huat Siti Mariam Yusof, Julia Mohd Idris, Zarina Abdul Latif, Wu, Loo Ling Wong, Ming Turner syndrome is one of the most common chromosomal abnormalities affecting newborn females. More than half of patients with Turner syndrome have a 45X karyotype. The rest of the patients may have structurally abnormal sex chromosomes or are mosaics with normal or abnormal sex chromosomes. Mosaicism with a second X sex chromosome is not usually of clinical significance. However, Turner syndrome patients having a second Y chromosome or Y chromosomal material are at risk of developing gonadoblastoma later in life. The aim of this study is to compare the results of conventional (karyotyping) and molecular cytogenetics (FISH), and discuss the advantages and limitations in the diagnosis of Turner syndrome. We also aim to compare the degree of mosaicism identified using conventional cytogenetics and FISH techniques. Conventional cytogenetics and FISH analyses were performed on eight peripheral blood samples of patients with Turner syndrome collected between 2004 and 2006. From this study, two out of eight patients with Turner syndrome were found to have the sex determining region on the Y chromosome (SRY) gene by FISH analysis. Our results showed that the rate of detection of mosaic cases in Turner syndrome was also increased to 88% after using the FISH technique. We concluded that FISH is more superior to conventional cytogenetics in the detection of the Y chromosomal material. FISH is also a quick and cost effective method in diagnosing Turner syndrome and assessing the degree of mosaicism Penerbit UKM 2008 Article PeerReviewed application/pdf en http://journalarticle.ukm.my/2004/1/Page_22_-_29.pdf Reena Rahayu Md Zin, and Sharifah Noor Akmal, and Zubaidah Zakaria, and Clarence, Ko Ching Huat and Siti Mariam Yusof, and Julia Mohd Idris, and Zarina Abdul Latif, and Wu, Loo Ling and Wong, Ming (2008) Identification of Y chromosomal material in turner syndrome by Fluorescence in Situ Hybridisation (FISH). Medicine & Health, 3 (1). pp. 22-29. ISSN 1823-2140 http://www.ppukm.ukm.my/ukmmcjournal/index.php
institution Universiti Kebangsaan Malaysia
building Perpustakaan Tun Sri Lanang Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Kebangsaan Malaysia
content_source UKM Journal Article Repository
url_provider http://journalarticle.ukm.my/
language English
description Turner syndrome is one of the most common chromosomal abnormalities affecting newborn females. More than half of patients with Turner syndrome have a 45X karyotype. The rest of the patients may have structurally abnormal sex chromosomes or are mosaics with normal or abnormal sex chromosomes. Mosaicism with a second X sex chromosome is not usually of clinical significance. However, Turner syndrome patients having a second Y chromosome or Y chromosomal material are at risk of developing gonadoblastoma later in life. The aim of this study is to compare the results of conventional (karyotyping) and molecular cytogenetics (FISH), and discuss the advantages and limitations in the diagnosis of Turner syndrome. We also aim to compare the degree of mosaicism identified using conventional cytogenetics and FISH techniques. Conventional cytogenetics and FISH analyses were performed on eight peripheral blood samples of patients with Turner syndrome collected between 2004 and 2006. From this study, two out of eight patients with Turner syndrome were found to have the sex determining region on the Y chromosome (SRY) gene by FISH analysis. Our results showed that the rate of detection of mosaic cases in Turner syndrome was also increased to 88% after using the FISH technique. We concluded that FISH is more superior to conventional cytogenetics in the detection of the Y chromosomal material. FISH is also a quick and cost effective method in diagnosing Turner syndrome and assessing the degree of mosaicism
format Article
author Reena Rahayu Md Zin,
Sharifah Noor Akmal,
Zubaidah Zakaria,
Clarence, Ko Ching Huat
Siti Mariam Yusof,
Julia Mohd Idris,
Zarina Abdul Latif,
Wu, Loo Ling
Wong, Ming
spellingShingle Reena Rahayu Md Zin,
Sharifah Noor Akmal,
Zubaidah Zakaria,
Clarence, Ko Ching Huat
Siti Mariam Yusof,
Julia Mohd Idris,
Zarina Abdul Latif,
Wu, Loo Ling
Wong, Ming
Identification of Y chromosomal material in turner syndrome by Fluorescence in Situ Hybridisation (FISH)
author_facet Reena Rahayu Md Zin,
Sharifah Noor Akmal,
Zubaidah Zakaria,
Clarence, Ko Ching Huat
Siti Mariam Yusof,
Julia Mohd Idris,
Zarina Abdul Latif,
Wu, Loo Ling
Wong, Ming
author_sort Reena Rahayu Md Zin,
title Identification of Y chromosomal material in turner syndrome by Fluorescence in Situ Hybridisation (FISH)
title_short Identification of Y chromosomal material in turner syndrome by Fluorescence in Situ Hybridisation (FISH)
title_full Identification of Y chromosomal material in turner syndrome by Fluorescence in Situ Hybridisation (FISH)
title_fullStr Identification of Y chromosomal material in turner syndrome by Fluorescence in Situ Hybridisation (FISH)
title_full_unstemmed Identification of Y chromosomal material in turner syndrome by Fluorescence in Situ Hybridisation (FISH)
title_sort identification of y chromosomal material in turner syndrome by fluorescence in situ hybridisation (fish)
publisher Penerbit UKM
publishDate 2008
url http://journalarticle.ukm.my/2004/1/Page_22_-_29.pdf
http://journalarticle.ukm.my/2004/
http://www.ppukm.ukm.my/ukmmcjournal/index.php
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