Narayanan Dhanya Lakshmi, Shukla Anju, Siddesh Anju Rani, Stephen Joshi, Srivastava Priyanka, Mandal Kausik, Phadke Shubha R
Department of Medical Genetics, Sanjay Gandhi Post Graduate Institute of Medical Sciences, Lucknow, Uttar Pradesh, 226014, India.
Indian J Pediatr. 2016 Sep;83(9):1003-5. doi: 10.1007/s12098-015-1947-4. Epub 2016 Feb 1.
Cartilage-hair hypoplasia is an autosomal recessive disorder, characterized by short stature, metaphyseal dysplasia, hypotrichosis and immunodeficiency. More than 90 different biallelic mutations in RMRP gene have been identified to cause this condition. Three cases previously reported from India showed novel mutations in RMRP gene. The authors report two unrelated cases with the more common g.70A > G mutation, stressing the need to screen for this mutation in Indian population having features of cartilage-hair hypoplasia.
软骨毛发发育不全是一种常染色体隐性疾病,其特征为身材矮小、干骺端发育异常、毛发稀少和免疫缺陷。已鉴定出RMRP基因中90多种不同的双等位基因突变可导致这种疾病。先前印度报道的3例病例显示RMRP基因存在新的突变。作者报告了2例携带更常见的g.70A>G突变的不相关病例,强调有必要在具有软骨毛发发育不全特征的印度人群中筛查这种突变。