With Turner's Syndrome, the females actually have 1 less chromosome, not an extra one or sometimes only part of the X chromosome is missing. Klinefelter's syndrome, 47, XXY, or XXY syndrome is a condition in which human males have an extra X chromosome. While females have an XX chromosomal makeup, and males an XY, affected individuals have at least two X chromosomes and at least one Y chromosome.
Turner syndrome is a genetic condition in females where one of the X chromosomes is partially or completely missing, resulting in short stature and infertility. Klinefelter syndrome is a genetic condition in males where there is an extra X chromosome, leading to infertility and possible developmental delays. Both conditions can impact fertility, but Klinefelter syndrome affects males and involves an extra chromosome, while Turner syndrome affects females and involves a missing chromosome.
Yes animals do sometimes have Turner's syndrome or Klinefelter's syndrome with similar characteristics as those observed in humans.
No, individuals with Turner syndrome typically have a karyotype of 45X. If a girl has a karyotype of 46XX, she would not be diagnosed with Turner syndrome.
Turner syndrome is a genetic disorder caused by a missing or incomplete X chromosome in females. It is characterized by specific physical features and can lead to health issues such as short stature and infertility.
Turner's disease is a rare genetic condition that can affect males, characterized by short stature and infertility due to chromosome abnormalities. This condition is also known as Noonan syndrome. Symptoms can vary but often include heart defects, developmental delays, and distinctive facial features. Treatment aims to manage symptoms and complications associated with the condition.
Yes, many babies born with Turner syndrome go on to live healthy lives with proper medical care and support. Early intervention and management can help address any potential health issues associated with the syndrome. Regular monitoring and treatment can help individuals with Turner syndrome lead full and independent lives.
Yes animals do sometimes have Turner's syndrome or Klinefelter's syndrome with similar characteristics as those observed in humans.
not a very bad (effective) symptom
Turner Syndrome is a genetic disorder that affects females only. It is caused by the absence of all or part of one of the X chromosomes. This condition is not passed down through family genetics, but occurs randomly.
No, individuals with Turner syndrome typically have a karyotype of 45X. If a girl has a karyotype of 46XX, she would not be diagnosed with Turner syndrome.
As a 19yr old female with Turner's Syndrome (diagnosed at 8yrs old), have never had any problems in school. There is usually no mental effect, however girls with turners may have problems with spatial problems and possibly math. However, I am in my second year of university, and have received an A in Linear Algebra, and have never had special treatment due to turners syndrome.
Turner syndrome is a genetic disorder caused by a missing or incomplete X chromosome in females. It is characterized by specific physical features and can lead to health issues such as short stature and infertility.
Turner's disease is a rare genetic condition that can affect males, characterized by short stature and infertility due to chromosome abnormalities. This condition is also known as Noonan syndrome. Symptoms can vary but often include heart defects, developmental delays, and distinctive facial features. Treatment aims to manage symptoms and complications associated with the condition.
yes. Not every girl/woman has issues with heart, or a webbed neck, for example. The syndrome affects each woman differently though short stature and infertility are almost always present.
Yes, many babies born with Turner syndrome go on to live healthy lives with proper medical care and support. Early intervention and management can help address any potential health issues associated with the syndrome. Regular monitoring and treatment can help individuals with Turner syndrome lead full and independent lives.
Turner syndrome is usually random and not inherited. It occurs when a female is born with a missing or incomplete X chromosome. In rare cases, Turner syndrome can be inherited if one parent carries a chromosomal abnormality.
Turner syndrome typically presents itself before birth or during early childhood. Symptoms may include short stature, webbed neck, and primary amenorrhea. Girls with Turner syndrome may also experience infertility and other health issues.
Yes, there are several types of Turner syndrome, including monosomy X, mosaic Turner syndrome, and partial X chromosome deletions. These variations in genetic makeup can affect the severity and presentation of symptoms in individuals with Turner syndrome.