
pmid: 11832602
handle: 1807/22563
Autosomal translocations are rare in the patients with ovarian dysgenesis. An 18-year-old female who presented with primary amenorrhoea had hypergonadotropic hypogonadism and streak ovaries with hypoplastic uterus. Karyotype analysis revealed a balanced autosomal translocation involving chromosomes 1 and 11. The probable role of autosomal translocations in ovarian dysgenesis has been discussed.
Adolescent, Chromosomes, Human, Pair 11, Ovary, Hypergonadotropic hypogonadism, Chromosome, Gonadal Dysgenesis, Translocation, Genetic, Chromosomes, Human, Pair 1, Karyotyping, Humans, Female, Amenorrhea, Gonadal dysgenesis
Adolescent, Chromosomes, Human, Pair 11, Ovary, Hypergonadotropic hypogonadism, Chromosome, Gonadal Dysgenesis, Translocation, Genetic, Chromosomes, Human, Pair 1, Karyotyping, Humans, Female, Amenorrhea, Gonadal dysgenesis
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