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Journal of pediatric endocrinology & metabolism : JPEM · 2015

Mode of initial presentation and chromosomal abnormalities in Irish patients with Turner syndrome: a single-centre experience.

СтатьяНазвание и аннотация: Перевод пока не подготовлен
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Mohamed Sarar, Roche Edna F, Hoey Hilary M C V

Аннотация

BACKGROUND: Age at diagnosis of girls with Turner syndrome (TS) is an important indicator of successful management. We determined the age, initial clinical presentation, and chromosomal abnormalities in patients with TS.

METHODS: This was a retrospective evaluation of the clinical and laboratory records of patients with TS.

RESULTS: Sixty-five patients with TS were identified; 40 (62%) were diagnosed after age 5 years. The main presenting features were short stature, delayed puberty, dysmorphic features, and neonatal lymphoedema. Chromosomal analysis of this cohort showed that 31 patients demonstrated mosaicism, while a 45,X karyotype was observed in 19. The remaining patients had variable abnormalities including deletion, translocation, isochromosome, and ring chromosome. Y-chromosome material was found in four cases.

CONCLUSIONS: Most patients with TS were diagnosed after age 5 years, had a varied clinical presentation, and had a wide range of chromosomal abnormalities.

Предметные рубрики MeSH

ИП Урсолов Владлен Сергеевич

ИНН 500118482352 · ОГРНИП 314500117700049

Реквизиты и контакты