Your browser doesn't support javascript.
loading
Montrer: 20 | 50 | 100
Résultats 1 - 1 de 1
Filtre
Ajouter des filtres








Gamme d'année
1.
Chinese Journal of Medical Genetics ; (6): 343-346, 2021.
Article Dans Chinois | WPRIM | ID: wpr-879582

Résumé

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.


Sujets)
Femelle , Humains , Protéine du syndrome X fragile/métabolisme , Syndrome du chromosome X fragile/génétique , Maladies ovariennes , Réserve ovarienne/génétique , Insuffisance ovarienne primitive/génétique , Répétitions de trinucléotides/génétique
SÉLECTION CITATIONS
Détails de la recherche