xxy genetic disorder

Yahoo answers: What does it mean if a baby has 1 Y chromosome in the male section, and 2 X chromosomes in the female section?

  • Biology

    It's Klinefelter's syndrome. :D It's one of chromosomal mutation which the structure of a whole chromosome or a set of chromosomes is altered in some way. Klinefelter's syndrome is a kind of...

Latest news about xxy genetic disorder

  • 46,XX Testicular Disorder of Sexual Development With SRY-Negative Caused ...

    Background 46,XX testicular disorder of sex development is a rare genetic syndrome, characterized by a complete or partial mismatch between genetic sex and phenotypic sex, which results in infertility because of the absence of the azoospermia factor
    Source: http://www.medscape.com/viewarticle/838426

  • Why are male calico cats so rare?

    This XXY combination can occur when there's an incomplete division of the male's XY chromosome pair at the time of fertilization — and it doesn't just happen in cats. It can occur in people too, resulting in a genetic disorder known as Klinefelter
    Source: http://www.mnn.com/family/pets/stories/why-are-male-calico-cats-so-rare

  • What Non-Invasive Prenatal Testing screens for

    NIPT provides information about specific fetal aneuploidies, or chromosomal abnormalities. According to the US National Coalition for Health Professional Education in Genetics, all laboratories offering NIPT report on Down's syndrome and Edwards
    Source: http://www.scmp.com/lifestyle/health/article/1680493/what-non-invasive-prenatal-testing-screens

  • Karolinska Team Demonstrates PCR-free NGS Method for Noninvasive Prenatal ...

    The amplification-free method accurately called all trisomies, however, in one case it called a sample as XY, contradicting quantitative fluorescence-PCR results that called it as XXY. To solve the discrepancy, the researchers obtained genomic DNA from
    Source: https://www.genomeweb.com/sequencing-technology/karolinska-team-demonstrates-pcr-free-ngs-method-noninvasive-prenatal

  • Klinefelter's syndrome: Adele Markham fought for 20 years to be a woman

    People with Klinefelter's syndrome are born with an extra sexual gene, so while boys are usually XY and girls are XX, Adele's genes are XXY. Although most boys with Klinefelter's syndrome grow up to live as men, some do develop female gender identities 
    Source: http://www.dailymail.co.uk/health/article-1346474/Klinefelters-syndrome-Adele-Markham-fought-20-years-woman.html

Images xxy genetic disorder

klinefelter syndrome, xxy .variants international awareness week:.
klinefelter syndrome, xxy .variants international awareness week:.

Syndrome, Klinefelter. Causes, symptoms, treatment Syndrome ...
Syndrome, Klinefelter. Causes, symptoms, treatment Syndrome ...

Genetic disorders
Genetic disorders

XXY Genetic Disorder (Klinefelter's Syndrome) - Jonah - Genetic
XXY Genetic Disorder (Klinefelter's Syndrome) - Jonah - Genetic

Xxy Genetic Disorder - a comprehensive view - Wellsphere
Xxy Genetic Disorder - a comprehensive view - Wellsphere

Other sites on the topic of xxy genetic disorder

  1. Klinefelter syndrome - Wikipedia, the free encyclopedia
    Klinefelter syndrome or Klinefelter's syndrome, also known as 47,XXY or XXY, is the set of symptoms resulting from a genetic disorder in which there is at least one ...
  2. Xxy Genetic Disorder - Understanding Weird Disorders
    XXY genetic disorder , or as it is more commonly known as Klinehelter’s Syndrome, is a sex chromosome problem that effects only the male population.
  3. Klinefelter syndrome - Genetics Home Reference
    Klinefelter syndrome affects 1 in 500 to 1,000 newborn males. Most variants of Klinefelter syndrome are much rarer, occurring in 1 in 50,000 or fewer newborns.
  4. Klinefelter Syndrome XXY Symptoms and Pictures
    Klinefelter Syndrome XXY chromosome genetic variation - Important Information and pictures. Symptoms include low testosterone and hypogonadism.
  5. xxy genetic disorder - lymes disease
    xxy genetic disorder. Verinata Health's Non-Invasive verifi® Prenatal Test Now Includes Unique Ability to Detect Additional Fetal Chromosomal Abnormalities