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婴儿系统性透明变性:焦特布尔“马利斯(农民)”群体起始密码子中的新型奠基者突变

Infantile Systemic Hyalinosis: Novel Founder Mutation in the Initiation Codon among "Malis (Farmers)" in Jodhpur.

作者信息

Soni Jai Prakash, Puri Ratna D, Jetha Kapil, Bhavani G S L, Chaudhary Monika, Kohli Sudha, Verma I C

机构信息

Genetic Clinic, Department of Pediatrics, Mother and Chlid Hospital, MDM Hospital, Shastri Nagar, Jodhpur, Rajasthan, India.

Institute of Genetics and Genomics, Sir Ganga Ram Hospital, Rajender Nagar, New Delhi, 110060, India.

出版信息

Indian J Pediatr. 2016 Nov;83(11):1341-1345. doi: 10.1007/s12098-016-2218-8. Epub 2016 Oct 18.

Abstract

Infantile systemic hyalinosis (OMIM 236490) is a progressive autosomal recessive disorder characterized by widespread deposition of hyaline material in many tissues leading to multiple subcutaneous skin nodules, gingival hypertrophy and joint contractures. The authors describe five children from four unrelated families, from the "mali (farmer)" community in Jodhpur, with the disorder. All of them had classical clinical features, and four died from severe infections between age of 7 mo to 3 y. Two affected children had the same, but novel mutation in the initiation codon, in homozygous form c.1 A > G; p. M1? in capillary morphogenesis protein-2 (CMG2), or ANTXR2 gene on chromosome 4q21.21. The other two parents had the same mutation in heterozygous form. It is likely that this is a founder mutation in this community.

摘要

婴儿全身性透明变性(OMIM 236490)是一种进行性常染色体隐性疾病,其特征是透明物质在许多组织中广泛沉积,导致多发性皮下皮肤结节、牙龈肥大和关节挛缩。作者描述了来自焦特布尔“马利(农民)”社区四个不相关家庭的五名患有该疾病的儿童。他们都具有典型的临床特征,其中四名在7个月至3岁之间死于严重感染。两名患病儿童在起始密码子处有相同但新的突变,纯合形式为c.1 A>G;p.M1?位于4q21.21染色体上的毛细血管形态发生蛋白2(CMG2)或ANTXR2基因中。另外两名父母为该突变的杂合形式。很可能这是该社区的一个奠基者突变。

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