A Case with Mosaic Ring Chromosome 18
Yazarlar (6)
Prof. Dr. Hale Samli Bursa Uludağ Üniversitesi, Türkiye
Doç. Dr. Asuman ÖZGÖZ Kastamonu Üniversitesi, Türkiye
Doç. Dr. Fadime Mutlu Içduygu Afyon Kocatepe Üniversitesi, Türkiye
Kuyas Hekimler
Afyon Kocatepe Üniversitesi, Türkiye
Yasar Sivaci
Afyon Kocatepe Üniversitesi, Türkiye
Necat Imirzalioǧlu
Hrs Women Hospital, Türkiye
Bildiri Türü Açık Erişim Tebliğ/Bildiri Bildiri Dili İngilizce
Bildiri Alt Türü Özet Metin Olarak Yayınlanan Tebliğ (Uluslararası Kongre/Sempozyum)
Bildiri Niteliği Alanında Hakemli Uluslararası Kongre/Sempozyum
DOI Numarası 10.12996/gmj.2013.26
Kongre Adı European Journal of Human Genetics Conference, 2009
Kongre Tarihi 23-05-2009 / 26-05-2009
Basıldığı Ülke Avusturya Basıldığı Şehir Vienna
Bildiri Linki https://www.eshg.org/fileadmin/www.eshg.org/abstracts/ESHG2009Abstracts.pdf
UAK Araştırma Alanları
Tıbbi Genetik
Özet
The classical mode of ring chromosome formation is by break forming in both arms of the affected chromosome, fusion of the breaking points and loss of the distal fragments. Ring chromosome of the chromosome 18 is relatively common among ring chromosomes and the rate of having typical clinical sings of 18p and 18q sydromes vary related to the length of the deletion in 18p and 18q. Ring 18 phenotype is characterised by growth retardation, mental retardation and nonspecific abnormalities, also facial dysmorphism and malformations may be observed. Our case referred with congenital malformation, motor mental retardation (MMR), short stature, high palate, pectus excavatus was evaluated genetically. GTL banding and FISH methods were performed for the metaphase plaques obtained from peripheral lymphocytes cultered for 72 hours. The karyotype of the case was detected to be 46,XX,r(18)[25]/46,XX[75] and confirmed by FISH analysis. © Copyright 2013 by Gazi University Medical Faculty.
Anahtar Kelimeler
Abnormality | Chromosome analysis | Ring chromosome 18
BM Sürdürülebilir Kalkınma Amaçları
Atıf Sayıları
Scopus 1
A Case with Mosaic Ring Chromosome 18

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