Ali Zafar, Babar Masroor Ellahi, Ahmad Jamil, Shah Sajjad Ali
Institute of Biochemistry and Biotechnology, University of Veterinary and Animal Sciences, Lahore, Pakistan.
Indian J Hum Genet. 2012 May;18(2):217-21. doi: 10.4103/0971-6866.100771.
Families with at least 2 or more individuals having hereditary hearing loss were enrolled from different areas of Khyber Pakhtoonkhwa, mainly from district Peshawar. Detailed history was taken from each family to minimize the presence of other abnormalities and environmental causes for deafness. Families were questioned about skin pigmentation, hair pigmentation, and problems relating to balance, vision, night blindness, thyroid, kidneys, heart, and infectious diseases like meningitis, antibiotic usage, injury, and typhoid. The pedigree structures were based upon interviews with multiple family members, and pedigrees of the enrolled families were drawn using Cyrillic program (version 2.1). All families showed recessive mode of inheritance. I studied 8 families of these 10. For linkage analyses, studies for DFNB1 locus, 3 STR markers (D13S175, D13S292, and D13S787) were genotyped using polyacrylamide gel electrophoresis (PAGE) and haplotypes were constructed to determined, linkage with DFNB1 locus. From a total of 8 families, a single family-10 showed linkage to DFNB1 locus.
从开伯尔-普赫图赫瓦省的不同地区,主要是白沙瓦地区招募了至少有两名或更多患有遗传性听力损失个体的家庭。对每个家庭进行了详细的病史询问,以尽量减少其他异常情况和导致耳聋的环境因素。询问了这些家庭有关皮肤色素沉着、头发色素沉着以及与平衡、视力、夜盲、甲状腺、肾脏、心脏等相关的问题,以及诸如脑膜炎、抗生素使用、受伤和伤寒等传染病情况。系谱结构基于对多名家庭成员的访谈,并使用西里尔程序(版本2.1)绘制了入选家庭的系谱。所有家庭均显示为隐性遗传模式。我研究了这10个家庭中的8个。为了进行连锁分析,对DFNB1位点、3个STR标记(D13S175、D13S292和D13S787)进行研究,使用聚丙烯酰胺凝胶电泳(PAGE)对其进行基因分型,并构建单倍型以确定与DFNB1位点的连锁关系。在总共8个家庭中,单个家庭10显示与DFNB1位点存在连锁关系。