Mundhofir Farmaditya E P, Nillesen Willy M, Van Bon Bregje W M, Smeets Dominique, Pfundt Rolph, van de Ven-Schobers Gaby, Ruiterkamp-Versteeg Martina, Winarni Tri I, Hamel Ben C J, Yntema Helger G, Faradz Sultana M H
Division of Human Genetics, Center for Biomedical Research, Faculty of Medicine Diponegoro University, Semarang, Indonesia ; Department of Human Genetics, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands.
Indian J Hum Genet. 2013 Apr;19(2):171-8. doi: 10.4103/0971-6866.116118.
Unbalanced subtelomeric chromosomal rearrangements are often associated with intellectual disability (ID) and malformation syndromes. The prevalence of such rearrangements has been reported to be 5-9% in ID populations.
To study the prevalence of subtelomeric rearrangements in the Indonesian ID population.
We tested 436 subjects with unexplained ID using multiplex ligation dependent probe amplification (MLPA) using the specific designed sets of probes to detect human subtelomeric chromosomal imbalances (SALSA P070 and P036D). If necessary, abnormal findings were confirmed by other MLPA probe kits, fluorescent in situ hybridization or Single Nucleotide Polymorphism array.
A subtelomeric aberration was identified in 3.7% of patients (16/436). Details on subtelomeric aberrations and confirmation analyses are discussed.
This is the first study describing the presence of subtelomeric rearrangements in individuals with ID in Indonesia. Furthermore, it shows that also in Indonesia such abnormalities are a prime cause of ID and that in developing countries with limited diagnostic services such as Indonesia, it is important and feasible to uncover the genetic etiology in a significant number of cases with ID.
亚端粒染色体重排失衡常与智力障碍(ID)及畸形综合征相关。据报道,此类重排在ID人群中的患病率为5% - 9%。
研究印度尼西亚ID人群中亚端粒重排的患病率。
我们使用多重连接依赖探针扩增技术(MLPA),采用特定设计的探针组(SALSA P070和P036D)检测人类亚端粒染色体失衡,对436例不明原因ID患者进行检测。如有必要,异常结果通过其他MLPA探针试剂盒、荧光原位杂交或单核苷酸多态性阵列进行确认。
在3.7%的患者(16/436)中发现了亚端粒畸变。文中讨论了亚端粒畸变的详细情况及确认分析。
这是第一项描述印度尼西亚ID个体中亚端粒重排情况的研究。此外,研究表明在印度尼西亚,此类异常也是ID的主要病因,并且在像印度尼西亚这样诊断服务有限的发展中国家,在大量ID病例中揭示遗传病因既重要又可行。