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1.
Eur J Neurol ; 27(2): 334-342, 2020 02.
Artigo em Inglês | MEDLINE | ID: mdl-31509304

RESUMO

BACKGROUND AND PURPOSE: Hypomyelinating leukodystrophies are a heterogeneous group of genetic disorders with a wide spectrum of phenotypes and a high rate of genetically unsolved cases. Bi-allelic mutations in NKX6-2 were recently linked to spastic ataxia 8 with hypomyelinating leukodystrophy. METHODS: Using a combination of homozygosity mapping, exome sequencing, and detailed clinical and neuroimaging assessment a series of new NKX6-2 mutations in a multicentre setting is described. Then, all reported NKX6-2 mutations and those identified in this study were combined and an in-depth analysis of NKX6-2-related disease spectrum was provided. RESULTS: Eleven new cases from eight families of different ethnic backgrounds carrying compound heterozygous and homozygous pathogenic variants in NKX6-2 were identified, evidencing a high NKX6-2 mutation burden in the hypomyelinating leukodystrophy disease spectrum. Our data reveal a phenotype spectrum with neonatal onset, global psychomotor delay and worse prognosis at the severe end and a childhood onset with mainly motor phenotype at the milder end. The phenotypic and neuroimaging expression in NKX6-2 is described and it is shown that phenotypes with epilepsy in the absence of overt hypomyelination and diffuse hypomyelination without seizures can occur. CONCLUSIONS: NKX6-2 mutations should be considered in patients with autosomal recessive, very early onset of nystagmus, cerebellar ataxia with hypotonia that rapidly progresses to spasticity, particularly when associated with neuroimaging signs of hypomyelination. Therefore, it is recommended that NXK6-2 should be included in hypomyelinating leukodystrophy and spastic ataxia diagnostic panels.


Assuntos
Deficiência Intelectual , Espasticidade Muscular , Atrofia Óptica , Ataxias Espinocerebelares , Criança , Proteínas de Homeodomínio , Humanos , Mutação , Fenótipo
2.
Toxicol Appl Pharmacol ; 222(1): 25-32, 2007 Jul 01.
Artigo em Inglês | MEDLINE | ID: mdl-17490695

RESUMO

This study is a result of an analysis of free and conjugated phytoestrogens daidzein, genistein, daidzin, genistin and coumesterol in human cord blood plasma using LCMS. Cord blood was collected from urban and rural populations of Malaysia (n=300) to establish a simple preliminary database on the levels of the analyzed compounds in the collected samples. The study also aimed to look at the levels of phytoestrogens in babies during birth as this may have a profound effect on the developmental process. The sample clean up was carried out by solid-phase extraction using C18 column and passed through DEAE sephadex gel before analysis by LCMS. The mean concentrations of total phytoestrogens were daidzein (1.4+/-2.9 ng/ml), genistein (3.7+/-2.8 ng/ml), daidzin (3.5+/-3.1 ng/ml), genistin (19.5+/-4.2 ng/ml) and coumesterol (3.3+/-3.3 ng/ml). Distribution of phytoestrogen was found to be higher in samples collected from rural areas compared to that of urban areas.


Assuntos
Sangue Fetal/química , Fitoestrógenos/sangue , Adulto , Coleta de Amostras Sanguíneas , Cromatografia Líquida de Alta Pressão , Cromatografia por Troca Iônica , DEAE-Dextrano , Feminino , Análise de Alimentos , Cromatografia Gasosa-Espectrometria de Massas , Humanos , Recém-Nascido , Isoflavonas/sangue , Escore Lod , Malásia , Troca Materno-Fetal , Gravidez , Padrões de Referência , População Rural , População Urbana
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