Cantlay A M, Shokrollahi K, Allen J T, Lunt P W, Newbury-Ecob R A, Steward C G
Department of Pathology and Microbiology, Bristol University, Southmead Hospital, Bristol, UK.
J Pediatr. 1999 Sep;135(3):311-5. doi: 10.1016/s0022-3476(99)70126-5.
Mutations have recently been identified in the G4.5 gene (Xq28), encoding the tafazzin protein, in patients with Barth syndrome. We performed mutational analysis in 5 families with suspected Barth syndrome. In 4 families a male child had all the cardinal features of this syndrome, and mutations of G4.5 were found in each case. A mutation was also found in a fifth family with an extensive history of early infant death from heart disease. The recognition of 5 unrelated families in 1 hospital during a 7-year period suggests that this disease may be underdiagnosed.
最近在患有Barth综合征的患者中,已确定在编码tafazzin蛋白的G4.5基因(Xq28)中存在突变。我们对5个疑似Barth综合征的家庭进行了突变分析。在4个家庭中,一名男童具有该综合征的所有主要特征,且在每个病例中均发现了G4.5突变。在第五个有早期婴儿因心脏病死亡广泛病史的家庭中也发现了一个突变。在7年时间里,同一家医院识别出5个无亲缘关系的家庭,这表明该疾病可能未得到充分诊断。