Turner Syndrome with Isochromosome Xq

[ X ]

Tarih

2020

Dergi Başlığı

Dergi ISSN

Cilt Başlığı

Yayıncı

Georg Thieme Verlag Kg

Erişim Hakkı

info:eu-repo/semantics/openAccess

Özet

Short stature and growth retardation in girls commonly occur in patients with Turner syndrome. We present a 19-year-old-girl with primary amenorrhea and growth retardation, who has a mosaic karyotype, 46X,i(Xq)[17]/45,X[8]. Classic Turner syndrome has a more severe phenotype than variant causes of Turner syndrome. We present a patient with 46,X,i(Xq) karyotype and compare the clinical and laboratory findings with the classic description of Turner syndrome. Our patient has normal social and psychomotor skills unlike previously reported cases in the literature. This case expands the phenotype-genotype description of Turner syndrome, which makes it an important contribution to the literature.

Açıklama

Anahtar Kelimeler

Turner Syndrome, Isochromosome, Phenotype, Genotype

Kaynak

Journal of Pediatric Genetics

WoS Q Değeri

N/A

Scopus Q Değeri

Cilt

9

Sayı

4

Künye