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1.
Clin Genet ; 88(4): e1-3, 2015 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-26138117

RESUMO

We report two Colombian siblings affected by overgrowth, intellectual disability and facial dysmorphism. Exome (via NGS) and Sanger sequencing revealed that biallelic sequence variants in a novel gene (HERC1) might be related to the disease pathogenesis. These results provide useful data for future genotype-phenotype correlations and for a molecular diagnosis of overgrowth.


Assuntos
Transtornos do Crescimento/genética , Fatores de Troca do Nucleotídeo Guanina/genética , Deficiência Intelectual/genética , Mutação , Análise Mutacional de DNA , Feminino , Estudos de Associação Genética , Genoma Humano , Transtornos do Crescimento/patologia , Humanos , Deficiência Intelectual/patologia , Masculino , Síndrome , Ubiquitina-Proteína Ligases
2.
Neurologia ; 30(3): 137-43, 2015 Apr.
Artigo em Inglês, Espanhol | MEDLINE | ID: mdl-24461309

RESUMO

INTRODUCTION: Genetic variance of attention deficit-hyperactivity disorder (ADHD) is a strong determinant of this disorder. The 40 base pairs (bp) variable number tandem repeat (VNTR) located in the 3' untranslated region (UTR) of DAT1 gene increases the expression of the dopamine transporter. Therefore, DAT1 has been associated with susceptibility to ADHD. OBJECTIVE: To determine the association between the VNTR of DAT1 and the phenotype of ADHD or its endophenotypes in a sample of children aged between 6 and 15 years from Bogotá. SUBJECTS AND METHODS: We selected 73 patients with ADHD and 54 controls. WISC test was applied in all subjects and executive functions were assessed. The VNTR of DAT1 was polymerase chain reaction-amplified. Data regarding population genetics and statistical analysis were obtained. Correlation and association tests between genotype and neuropsychological testing were performed. RESULTS: The DAT1 polymorphism was not associated with ADHD (P=.85). Nevertheless, the 10/10 genotype was found to be correlated with the processing speed index (P<.05). In the hyperactivity subtype, there was a genotypic correlation with some subtests of executive function (cognitive flexibility) (P≤.01). In the combined subtype, the 10/10 genotype was associated with verbal comprehension index of WISC (P<.05). CONCLUSIONS: A correlation was found between DAT1 VNTR and the subtest "processing speed index" of WISC and the subtest "cognitive flexibility" of executive functions. To our knowledge, this is the first report to assess DAT1 gene in a Colombian population.


Assuntos
Transtorno do Deficit de Atenção com Hiperatividade/genética , Proteínas da Membrana Plasmática de Transporte de Dopamina/genética , Endofenótipos , Regiões 3' não Traduzidas/genética , Adolescente , Criança , Colômbia , Proteínas da Membrana Plasmática de Transporte de Dopamina/metabolismo , Feminino , Genótipo , Humanos , Masculino , Repetições Minissatélites/genética , Testes Neuropsicológicos , Polimorfismo Genético
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