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一例伴有FGFR3基因R248C突变的I型致死性骨发育不全病例。

A case of thanatophoric dysplasia type I with an R248C mutation in the FGFR3 gene.

作者信息

Noe Eun Jung, Yoo Han Wook, Kim Kwang Nam, Lee So Yeon

机构信息

Department of Pediatrics, College of Medicine, Hallym University, Seoul, Korea.

出版信息

Korean J Pediatr. 2010 Dec;53(12):1022-5. doi: 10.3345/kjp.2010.53.12.1022. Epub 2010 Dec 31.

Abstract

Thanatophoric dysplasia (TD) is a short-limb neonatal dwarfism syndrome that is usually lethal in the perinatal period. It is characterized by shortening of the limbs, severely small thorax, large head with a prominent forehead, macrocephaly, curved femur, and flattened vertebral bodies. These malformations result from the mutation in fibroblast growth factor receptor 3 (FGFR-3) gene which is located on the short arm of chromosome 4. A definite diagnosis should be established by molecular genetic analysis to find out the abnormal mutations in the FGFR3 gene. We confirmed by detection of a R248C mutation in the FGFR3 gene in DNA analysis.

摘要

致死性侏儒症(TD)是一种短肢新生儿侏儒症综合征,通常在围产期致死。其特征为四肢短小、胸廓严重狭小、头部大且前额突出、巨头畸形、股骨弯曲以及椎体扁平。这些畸形是由位于4号染色体短臂上的成纤维细胞生长因子受体3(FGFR - 3)基因突变所致。应通过分子遗传学分析来确定诊断,以找出FGFR3基因中的异常突变。我们通过DNA分析检测到FGFR3基因中的R248C突变,从而得以证实。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0891/3021729/8c7728fc3f5a/kjped-53-1022-g001.jpg

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