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  2. Klinefelter syndrome - Wikipedia

    en.wikipedia.org/wiki/Klinefelter_syndrome

    Klinefelter syndrome is not an inherited condition. The extra X chromosome comes from the mother in approximately 50% of the cases. Maternal age is the only known risk factor. Women at 40 years have a four-times-higher risk of a child with Klinefelter syndrome than women aged 24 years. [14] [34] [35]

  3. XYY syndrome - Wikipedia

    en.wikipedia.org/wiki/XYY_syndrome

    XYY syndrome, also known as Jacobs syndrome, is an aneuploid genetic condition in which a male has an extra Y chromosome. [1] There are usually few symptoms. [ 2 ] These may include being taller than average and an increased risk of learning disabilities .

  4. XXXXY syndrome - Wikipedia

    en.wikipedia.org/wiki/XXXXY_syndrome

    It can be considered a form or variant of Klinefelter syndrome (47,XXY). [11] Individuals with this syndrome are typically mosaic, being 49,XXXXY/48, XXXX. [4] It is genetic but not hereditary, meaning that while the genes of the parents cause the syndrome, there is a small chance of more than one child having the syndrome.

  5. Trisomy X - Wikipedia

    en.wikipedia.org/wiki/Trisomy_X

    The autoimmune disease ... suggests a life expectancy ... In 2022 Trisomy X was included alongside XYY at the 3rd International Workshop on Klinefelter Syndrome, ...

  6. Trisomy - Wikipedia

    en.wikipedia.org/wiki/Trisomy

    XXX (Triple X syndrome) XXY (Klinefelter syndrome) XYY (Jacobs syndrome) Compared to trisomy of the autosomal chromosomes, trisomy of the sex chromosomes normally has less severe consequences. Individuals may show few or no symptoms and have a normal life expectancy. [4]

  7. List of genetic disorders - Wikipedia

    en.wikipedia.org/wiki/List_of_genetic_disorders

    Klinefelter syndrome: X C Neurofibromatosis: 17q/22q/? Phenylketonuria: 12q P Polycystic kidney disease: 16 or 4 P Prader–Willi syndrome: 15q DCP Scheuermann's disease: 1q21-q22 or 7q22 Sickle cell disease: 11p P Spinal muscular atrophy: 5q DP Tay–Sachs disease: 15q P Turner syndrome: X C

  8. What is Angelman Syndrome, the disease affecting Colin ...

    www.aol.com/angelman-syndrome-disease-affecting...

    "Angelman syndrome shares symptoms and characteristics with other disorders including autism, cerebral palsy and Prader-Willi syndrome," read the Angelman Syndrome Foundation website. "People with ...

  9. XXYY syndrome - Wikipedia

    en.wikipedia.org/wiki/XXYY_syndrome

    48,XXYY syndrome is a condition related to the X and Y chromosomes (the sex chromosomes). People normally have 46 chromosomes in each cell.Two of the 46 chromosomes, known as X and Y, are called sex chromosomes because they help determine whether a person will develop male or female sex characteristics.