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Turner Syndrome with Isochromosome Xq
Author(s) -
Gülbahar Güzel Erdal,
Mahmut Balkan
Publication year - 2019
Publication title -
journal of pediatric genetics
Language(s) - English
Resource type - Journals
eISSN - 2146-4596
pISSN - 2146-460X
DOI - 10.1055/s-0039-3399496
Subject(s) - turner syndrome , short stature , karyotype , turner's syndrome , girl , pediatrics , primary amenorrhea , x chromosome , gonadal dysgenesis , medicine , genetics , gynecology , biology , chromosome , gene
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.

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