Cytogenetics and cell genetics · 2000
An SRY-negative 47,XXY mother and daughter.
Клинический случайСтатьяНазвание и аннотация: Перевод в очереди
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Röttger S, Schiebel K, Senger G, Ebner S, Schempp W, Scherer G
Аннотация
Females with XY gonadal dysgenesis are sterile, due to degeneration of the initially present ovaries into nonfunctional streak gonads. Some of these sex-reversal cases can be attributed to mutation or deletion of the SRY gene. We now describe an SRY-deleted 47,XXY female who has one son and two daughters, and one of her daughters has the same 47,XXY karyotype. PCR and FISH analysis revealed that the mother carries a structurally altered Y chromosome that most likely resulted from an aberrant X-Y interchange between the closely related genomic regions surrounding the gene pair PRKX and PRKY on Xp22.3 and Yp11.2, respectively. As a consequence, Yp material, including SRY, has been replaced by terminal Xp sequences up to the PRKX gene. The fertility of the XXY mother can be attributed to the presence of the additional X chromosome that is missing in XY gonadal dysgenesis females. To our knowledge, this is the first human XXY female described who is fertile.
Предметные рубрики MeSH
DNA-Binding ProteinsDisorders of Sex DevelopmentFemaleFertilityHumansIn Situ Hybridization, FluorescenceKaryotypingKlinefelter SyndromeMaleNuclear FamilyNuclear ProteinsPregnancyPrenatal DiagnosisRecombination, GeneticSequence DeletionSex Chromosome AberrationsSex-Determining Region Y ProteinTranscription FactorsX ChromosomeY Chromosome