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Analysis of FMR1 gene CGG repeats among patients with diminished ovarian reserve / 中华医学遗传学杂志
Chinese Journal of Medical Genetics ; (6): 343-346, 2021.
Artículo en Chino | WPRIM | ID: wpr-879582
ABSTRACT
OBJECTIVE@#To explore the correlation between Fragile X mental retardation gene-1 (FMR1) gene CGG repeats with diminished ovarian reserve (DOR).@*METHODS@#For 214 females diagnosed with DOR, DNA was extracted from peripheral blood samples. FMR1 gene CGG repeats were determined by PCR and capillary electrophoresis.@*RESULTS@#Three DOR patients were found to carry FMR1 premutations, and one patient was found to carry gray zone FMR1 repeats. After genetic counseling, one patient and the sister of another patient, both carrying FMR1 permutations, conceived naturally. Prenatal diagnosis showed that both fetuses have carried FMR1 permutations.@*CONCLUSION@#FMR1 gene permutation may be associated with DOR. Determination of FMR1 gene CGG repeats in DOR patients can provide a basis for genetic counseling and guidance for reproduction.
Asunto(s)
Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Enfermedades del Ovario / Insuficiencia Ovárica Primaria / Repeticiones de Trinucleótidos / Proteína de la Discapacidad Intelectual del Síndrome del Cromosoma X Frágil / Reserva Ovárica / Síndrome del Cromosoma X Frágil Tipo de estudio: Guía de Práctica Clínica Límite: Femenino / Humanos Idioma: Chino Revista: Chinese Journal of Medical Genetics Año: 2021 Tipo del documento: Artículo

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Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Enfermedades del Ovario / Insuficiencia Ovárica Primaria / Repeticiones de Trinucleótidos / Proteína de la Discapacidad Intelectual del Síndrome del Cromosoma X Frágil / Reserva Ovárica / Síndrome del Cromosoma X Frágil Tipo de estudio: Guía de Práctica Clínica Límite: Femenino / Humanos Idioma: Chino Revista: Chinese Journal of Medical Genetics Año: 2021 Tipo del documento: Artículo