Turner Syndrome with Isochromosome Xq

被引:4
作者
Erdal, Gulbahar Guzel [1 ]
Balkan, Mahmut [1 ]
机构
[1] Dicle Univ, Dept Med Biol & Genet, Fac Med, TR-21010 Diyarbakir, Turkey
关键词
Turner syndrome; isochromosome; phenotype; genotype;
D O I
10.1055/s-0039-3399496
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
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.
引用
收藏
页码:243 / 245
页数:3
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