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PMID: 20573177 已发表 · ppublish 英语

Maternal uniparental isodisomy is responsible for serious molybdenum cofactor deficiency.

Developmental medicine and child neurology ·第 52 卷 ·第 9 期 ·2010-09-27

Gümüş Hakan, Ghesquiere Stijn, Per Hüseyin, Kondolot Meda, Ichida Kimiyoshi, Poyrazoğlu Gamze, Kumandaş Sefer, Engelen John, Dundar Munis, Cağlayan Ahmet Okay

摘要

Molybdenum cofactor (MoCo) deficiency is a rare autosomal recessive inherited metabolic disorder resulting in the combined deficiency of aldehyde oxidase, xanthine dehydrogenase, and sulfite oxidase. We report a male infant with MoCo deficiency whose clinical findings consisted of microcephaly, intractable seizures soon after birth, feeding difficulties, and developmental delay. Sequencing of MOCS1, MOCS2, and GEPH genes, and single nucleotide polymorphism genotyping array analysis showed, to our knowledge, unusual inheritance of MoCo deficiency/maternal uniparental isodisomy for the first time in the literature. At 10 months of age, he now has microcephaly and developmental delay, and his seizures are controlled with phenobarbital, clonozepam, and vigabatrin therapy.

文献信息
期刊
Developmental medicine and child neurology
期刊简称
Dev Med Child Neurol
发表日期
2010-09-27
收录日期
2010-08-24
更新日期
2010-08-24
语言
英语
国家/地区
England
NLM ID
0006761
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