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karyotype$42097$ - перевод на испанский

GENETIC CONDITION IN WHICH A MALE HAS AN EXTRA Y CHROMOSOME

47,XYY; 47,XYY syndrome; XYY Karyotype; XYY karyotype; XYY-Trisomy; Xyy syndrome; XYY; Supermale syndrome; Karyotype 47,XYY; Jacobs syndrome; 47 xyy syndrome; Jacob's Syndrome; YY syndrome; Jacob syndrome; Jacob's syndrome; Xyy karyotype; Double Y Syndrome; Xyy; XYY chromosome; XYY chromosomes; Superman syndrome; Extra Y chromosome

karyotype

n. cariotipo (Gen. - el conjunto de propiedades del cromosoma en un sexo dado)

Turner syndrome

CHROMOSOMAL DISORDER IN WHICH A FEMALE IS PARTIALLY OR COMPLETELY MISSING AN X CHROMOSOME

Turner's syndrome; Turner Syndrome; 45,X; XO syndrome; Turner's Syndrome; Gonadal dysgenesis Turner type; Bonnevie-Ullrich syndrome; Turners syndrome; Turners Syndrome; Karyotype 45,X; 45,X karyotype; Turner's; Turner disease; Ullrich-Turner syndrome; Bonnevie-Ulrich-Turner syndrome; Ulrich-Turner Syndrome; Bonnevie-Ullrich-Turner syndrome; Turner syndrome (Gonadal dysgenesis); Bonnevie Ullrich Turner syndrome; Single X syndrome; X syndrome; Bonnevie-Ulrich-Turner Syndrome; Bonnevie-Ulrich-Turner's Syndrome; Monosomy X; Partial anomalous venous drainage; Bonnevie–Ullrich–Turner syndrome; Bonnevie–Ullrich syndrome; Ring-X Turner Syndrome; Ring-X Turner syndrome; 45,X0

(Medicina) El síndrome de Turner, síndrome genético que aparece principalmente en mujeres (se caracteriza por la falta del cromosoma "X" y causa entre otros infertilidad)

Определение

karyotype

['kar??(?)t??p]

¦ noun Biology & Medicine the number and visual appearance of the chromosomes in the cell nuclei of an organism.

Derivatives

karyotypic adjective

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Википедия

XYY syndrome

XYY syndrome, also known as Jacobs syndrome, is an aneuploid genetic condition in which a male has an extra Y chromosome. There are usually few symptoms. These may include being taller than average, acne, and an increased risk of learning disabilities. The person is generally otherwise normal, including typical rates of fertility.

The condition is generally not inherited but rather occurs as a result of a random event during sperm development. Diagnosis is by a chromosomal analysis, but most of those affected are not diagnosed within their lifetime. There are 47 chromosomes, instead of the usual 46, giving a 47,XYY karyotype.

Treatment may include speech therapy or extra help with schoolwork, however outcomes are generally positive. The condition occurs in about 1 in 1,000 male births. Many people with the condition are unaware that they have it. The condition was first described in 1961.

https://en.wikipedia.org/wiki/XYY syndrome