Klinefelter's syndrome karyotype 47,XXY | Wellcome Collection

47 Xxy Karyotype

Klinefelter syndrome (ks), also known as 47,xxy, is a chromosome anomaly where a male has an extra x chromosome The remaining 10% of individuals have karyotypes that contain additional x chromosomes (ie, 48,xxxy and 49,xxxxy) or mosaicism consisting of 2 or more cell lines.9 most individuals with 47,xxy mosaicism have an xy cell line (eg, 47,xxy/46,xy), typically in conjunction with a less pronounced phenotype and are diagnosed at a later age, often.

[10] the complications commonly include infertility and small, poorly functioning testicles (if present). May have cryptorchidism, micropenis, hypospadias 47,xxy (klinefelter syndrome) is a chromosomal variation in males where one extra x chromosome is present which then results in a 47,xxy

Klinefelter's syndrome karyotype 47,XXY | Wellcome Collection

The extra x chromosome typically affects physical, neurodevelopmental, behavioral and neurocognitive functioning.

Klinefelter syndrome description klinefelter syndrome, also called 47,xxy, is a chromosomal condition that affects male development

The signs and symptoms of klinefelter syndrome vary In some cases, the features are so mild that the condition is not diagnosed until puberty or adulthood. 48,xxxy or 48,xxyy), structurally abnormal x chromosome (e.g 47,xxy/46,xy) make up approximately in the remaining 10.

Key points klinefelter syndrome (ks) Longer cag repeats in androgen receptor gene correlate with severity

Klinefelter's syndrome karyotype 47,XXY | Wellcome Collection
Klinefelter's syndrome karyotype 47,XXY | Wellcome Collection

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A karyotype of 47,XXY. | Download Scientific Diagram
A karyotype of 47,XXY. | Download Scientific Diagram

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Xxy Karyotype
Xxy Karyotype

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