Department of Clinical Genetics, Erasmus MC, Rotterdam, The Netherlands.
Am J Med Genet A. 2012 Jun;158A(6):1472-6. doi: 10.1002/ajmg.a.35365. Epub 2012 May 14.
Mutations in the ARX gene, at Xp22.3, cause several disorders, including infantile spasms, X-linked lissencephaly with abnormal genitalia (XLAG), callosal agenesis and isolated intellectual disability. Genotype/phenotype studies suggested that polyalanine tract expansion is associated with non-malformative phenotypes, while missense and nonsense mutations cause cerebral malformations, however, patients with structural normal brain and missense mutations have been reported. We report on a male patient born with cleft lip and palate who presented with infantile spasms and hemiplegia. MRI showed agenesis of corpus callosum (ACC), an interhemispheric cyst, periventricular nodular heterotopia (PVNH), and extensive left frontal polymicrogyria (PMG). Sequencing of the ARX gene in the patient identified a six basepair insertion (c.335ins6, exon 2). The insertion leads to a two-residue expansion of the first polyalanine tract and was described previously in a family with non-syndromic X-linked mental retardation. To our knowledge, ARX mutation causing PMG and PVNH is unique, but the spasms and ACC are common in ARX mutations. Clinicians should be aware of the broad clinical range of ARX mutations, and further studies are necessary to investigate the association with PMG and PVNH and to identify possible modifying factors.
ARX 基因突变位于 Xp22.3,可导致多种疾病,包括婴儿痉挛、伴生殖器异常的 X 连锁无脑回畸形(XLAG)、胼胝体发育不全和孤立性智力障碍。基因型/表型研究表明,多聚丙氨酸链扩展与非畸形表型相关,而错义和无义突变导致脑畸形,然而,已有报道称具有结构正常大脑和错义突变的患者。我们报告了一名男性患者,出生时患有唇裂和腭裂,表现为婴儿痉挛和偏瘫。MRI 显示胼胝体发育不全(ACC)、半球间囊肿、脑室周围结节性异位(PVNH)和广泛的左侧额部多小脑回(PMG)。对患者 ARX 基因的测序发现了一个六碱基插入(c.335ins6,外显子 2)。该插入导致第一个多聚丙氨酸链的两个残基扩展,先前在一个非综合征性 X 连锁智力障碍的家族中已有描述。据我们所知,导致 PMG 和 PVNH 的 ARX 突变是独特的,但痉挛和 ACC 在 ARX 突变中很常见。临床医生应该意识到 ARX 突变的广泛临床范围,需要进一步研究以调查与 PMG 和 PVNH 的关联,并确定可能的修饰因子。