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1.
Am J Hum Genet ; 90(4): 701-7, 2012 Apr 06.
Artículo en Inglés | MEDLINE | ID: mdl-22424600

RESUMEN

Kohlschütter-Tönz syndrome (KTS) is an autosomal-recessive disease characterized by the combination of epilepsy, psychomotor regression, and amelogenesis imperfecta. The molecular basis has not yet been elucidated. Here, we report that KTS is caused by mutations in ROGDI. Using a combination of autozygosity mapping and exome sequencing, we identified a homozygous frameshift deletion, c.229_230del (p.Leu77Alafs(∗)64), in ROGDI in two affected individuals from a consanguineous family. Molecular studies in two additional KTS-affected individuals from two unrelated Austrian and Swiss families revealed homozygosity for nonsense mutation c.286C>T (p.Gln96(∗)) and compound heterozygosity for the splice-site mutations c.531+5G>C and c.532-2A>T in ROGDI, respectively. The latter mutation was also found to be heterozygous in the mother of the Swiss affected individual in whom KTS was reported for the first time in 1974. ROGDI is highly expressed throughout the brain and other organs, but its function is largely unknown. Possible interactions with DISC1, a protein involved in diverse cytoskeletal functions, have been suggested. Our finding that ROGDI mutations cause KTS indicates that the protein product of this gene plays an important role in neuronal development as well as amelogenesis.


Asunto(s)
Amelogénesis Imperfecta/genética , Demencia/genética , Epilepsia/genética , Proteínas de la Membrana/genética , Mutación , Proteínas Nucleares/genética , Secuencia de Bases , Mapeo Cromosómico , Exoma , Exones , Femenino , Heterocigoto , Homocigoto , Humanos , Lactante , Masculino , Datos de Secuencia Molecular
2.
Lancet ; 367(9519): 1352-61, 2006 Apr 22.
Artículo en Inglés | MEDLINE | ID: mdl-16631914

RESUMEN

Despite worldwide public-health campaigns recommending periconceptional daily supplementation of synthetic folic acid to reduce the risk of neural tube defects, many women are not following these recommendations. At the same time, in most European countries no decline in defects has been recorded in recent years. Vulnerable groups are those with a low standard of education, young people, and women with unplanned pregnancies. Furthermore, in most countries without mandatory fortification, the general population is not consuming the recommended 0.4 mg of food folate per day. Voluntary fortification improves the situation, but does not reach all parts of the population. In the USA, Canada, and Chile, mandatory fortification of flour substantially improved folate and homocysteine status, and neural tube defects rates fell by between 31% and 78%. Nevertheless, many countries do not choose mandatory folic acid fortification, in part because expected additional health benefits are not yet scientifically proven in clinical trials, in part because of feared health risks, and because of the issue of freedom of choice. Thus, additional creative public-health approaches need to be developed to prevent neural tube defects and improve the folate status of the general population.


Asunto(s)
Dieta , Ácido Fólico/uso terapéutico , Defectos del Tubo Neural/prevención & control , Salud Pública , Disrafia Espinal/prevención & control , Adulto , Femenino , Ácido Fólico/administración & dosificación , Alimentos Fortificados , Educación en Salud , Humanos , Recién Nacido , Embarazo
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