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携带突变型鸟氨酸转氨甲酰酶(OTC)等位基因Arg40His的男性患者的表型变异性,范围从预后不良的儿童到无症状的老年成年人。

Phenotypic variability in male patients carrying the mutant ornithine transcarbamylase (OTC) allele, Arg40His, ranging from a child with an unfavourable prognosis to an asymptomatic older adult.

作者信息

Matsuda I, Matsuura T, Nishiyori A, Komaki S, Hoshide R, Matsumoto T, Funakoshi M, Kiwaki K, Endo F, Hata A, Shimadzu M, Yoshino M

机构信息

Department of Paediatrics, School of Medicine, Kumamoto University, Japan.

出版信息

J Med Genet. 1996 Aug;33(8):645-8. doi: 10.1136/jmg.33.8.645.

Abstract

In five different Japanese families, we identified six male hemizygotes (aged 6, 9, 15, 17, 56, and 65 years) and a putative candidate (aged 48 years), carrying a mutant allele of the ornithine transcarbamylase (OTC) gene, a G to A substitution at nucleotide 119 in exon 2 generating histidine in place of arginine. OTC activity in the necropsied liver tissue was reduced to approximately 12% of the control and that of COS 1 cells transfected with Arg40His OTC cDNA was 10.2 +/- 1.8% of the control transfected with wild type OTC cDNA. Clinical features ranged from death during a hyperammonaemic attack (a 9 year old) to a 65 year old asymptomatic man. We consider that the amount of protein ingested by these subjects may be one predisposing factor leading to the manifestation of this disease.

摘要

在五个不同的日裔家庭中,我们鉴定出六名男性半合子(年龄分别为6岁、9岁、15岁、17岁、56岁和65岁)以及一名疑似患者(48岁),他们携带鸟氨酸转氨甲酰酶(OTC)基因的突变等位基因,该突变是外显子2中第119位核苷酸由G替换为A,导致精氨酸被组氨酸取代。尸检肝脏组织中的OTC活性降至对照的约12%,而用Arg40His OTC cDNA转染的COS 1细胞的活性是用野生型OTC cDNA转染的对照的10.2±1.8%。临床特征从高氨血症发作时死亡(一名9岁患者)到一名65岁无症状男性不等。我们认为这些受试者摄入的蛋白质量可能是导致该疾病表现的一个易感因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2d0/1050697/b0fb4e9a81a6/jmedgene00262-0014-a.jpg

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