Genetic diagnosis for a Chinese Han family with hereditary multiple osteochondromas.
- Author:
Xue-shuang HUANG
1
;
Jian-shu LIU
;
Hai-ou JIANG
;
Qing-li QUAN
;
Xiao-qing SHEN
Author Information
- Publication Type:Journal Article
- MeSH: Asian Continental Ancestry Group; genetics; Child; Exostoses, Multiple Hereditary; diagnosis; genetics; Female; Heterozygote; Humans; Male; Mutation; N-Acetylglucosaminyltransferases; genetics; Pedigree
- From: Chinese Journal of Medical Genetics 2013;30(6):645-648
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo identify the genetic cause for a Chinese Han family affected with hereditary multiple osteochondromas.
METHODSTwo patients, five unaffected relatives of the family and 100 unrelated healthy controls were collected. The coding sequences and intron/exon boundaries of EXT1 gene were amplified with polymerase chain reaction (PCR) and sequenced.
RESULTSA heterozygous c.600G>A (p.Trp200X) mutation in exon 1 of the EXT1 gene was detected in the patients. The same mutation was not found in unaffected family members and 100 healthy controls.
CONCLUSIONThe hereditary multiple osteochondromas in the family is caused by a nonsense mutation (p.Trp200X) in the EXT1 gene.
