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1.
Hum Mol Genet ; 25(18): 4062-4079, 2016 09 15.
Artículo en Inglés | MEDLINE | ID: mdl-27466185

RESUMEN

The Acadian variant of Fanconi Syndrome refers to a specific condition characterized by generalized proximal tubular dysfunction from birth, slowly progressive chronic kidney disease and pulmonary interstitial fibrosis. This condition occurs only in Acadians, a founder population in Nova Scotia, Canada. The genetic and molecular basis of this disease is unknown. We carried out whole exome and genome sequencing and found that nine affected individuals were homozygous for the ultra-rare non-coding variant chr8:96046914 T > C; rs575462405, whereas 13 healthy siblings were either heterozygotes or lacked the mutant allele. This variant is located in intron 2 of NDUFAF6 (NM_152416.3; c.298-768 T > C), 37 base pairs upstream from an alternative splicing variant in NDUFAF6 chr8:96046951 A > G; rs74395342 (c.298-731 A > G). NDUFAF6 encodes NADH:ubiquinone oxidoreductase complex assembly factor 6, also known as C8ORF38. We found that rs575462405-either alone or in combination with rs74395342-affects splicing and synthesis of NDUFAF6 isoforms. Affected kidney and lung showed specific loss of the mitochondria-located NDUFAF6 isoform and ultrastructural characteristics of mitochondrial dysfunction. Accordingly, affected tissues had defects in mitochondrial respiration and complex I biogenesis that were corrected with NDUFAF6 cDNA transfection. Our results demonstrate that the Acadian variant of Fanconi Syndrome results from mitochondrial respiratory chain complex I deficiency. This information may be used in the diagnosis and prevention of this disease in individuals and families of Acadian descent and broadens the spectrum of the clinical presentation of mitochondrial diseases, respiratory chain defects and defects of complex I specifically.


Asunto(s)
Complejo I de Transporte de Electrón/genética , Síndrome de Fanconi/genética , Mitocondrias/metabolismo , Enfermedades Mitocondriales/genética , Proteínas Mitocondriales/genética , Adulto , Alelos , Canadá , Mapeo Cromosómico , Exoma/genética , Síndrome de Fanconi/patología , Femenino , Predisposición Genética a la Enfermedad , Heterocigoto , Homocigoto , Humanos , Riñón/metabolismo , Riñón/patología , Pulmón/metabolismo , Pulmón/patología , Masculino , Persona de Mediana Edad , Mitocondrias/patología , Enfermedades Mitocondriales/metabolismo , Enfermedades Mitocondriales/patología , Mutación
2.
CANNT J ; 15(2): 42-7, 2005.
Artículo en Francés | MEDLINE | ID: mdl-16050364

RESUMEN

The purpose of this quasi-experimental study was to compare two teaching methods of a predialysis educational program, namely on-site and by distance. This program was offered to patients with chronic kidney disease (CKD) stage 3. The experimental group one received the on-site program, whereas the experimental group two received the teaching program by distance. This study uses a pre-test post-test design. Measures included a Sociodemographic Information Form, the Degree of Knowledge Integration (Aucoin-Gallant, 1998), and the Knowledge Satisfaction Scale (Aucoin, 1998). In this study, both groups are homogenous from a sociodemographic perspective and have similar creatinine clearance values. Findings demonstrate an increase with knowledge integration and satisfaction with knowledge that is statistically significant for both groups of subjects. Participants in group two learned as much as participants in group one. This study highlights that knowledge integration leads to satisfaction in both groups of subjects. The results demonstrate that predialysis teaching delivered on-site or by distance promotes knowledge integration for patients with CKD stage 3.


Asunto(s)
Educación a Distancia , Educación del Paciente como Asunto/métodos , Diálisis Renal/enfermería , Anciano , Femenino , Humanos , Masculino , Persona de Mediana Edad
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