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Gynecol Endocrinol ; 36(9): 829-834, 2020 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-32063091

RESUMEN

Oocyte maturation defect is a challenging situation in the management of infertility, the etiology may be related to endocrine causes, protocols used in ovarian stimulation, oocyte intrinsic defects or procedures in embryology laboratory. We report three Mexican females in treatment for primary infertility with non-mature oocytes after ovary stimulation and oocyte capture in whom a genetic diagnosis of TUBB8-oocyte maturation defect was revealed by exome sequencing. Two couples achieved pregnancies though oocyte donation after establishing the genetic etiology. Our results expand the role of TUBB8-disorders in patients of non-Asian ethnicity. Oocyte maturation defects of monogenic origin are a growing group of disorders that endocrinologists and reproductive medicine specialists should be aware in order to provide referral to genetics for establish a correct and opportune diagnosis.


Asunto(s)
Enfermedades Genéticas Congénitas/terapia , Infertilidad Femenina/diagnóstico , Infertilidad Femenina/terapia , Oogénesis/genética , Tubulina (Proteína)/genética , Adulto , Análisis Mutacional de ADN , Femenino , Enfermedades Genéticas Congénitas/diagnóstico , Enfermedades Genéticas Congénitas/epidemiología , Humanos , Infertilidad Femenina/epidemiología , Infertilidad Femenina/genética , México , Mutación , Linaje , Embarazo , Pronóstico , Técnicas Reproductivas Asistidas/estadística & datos numéricos , Resultado del Tratamiento
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