Hemophilia
Sickle-Cell Anemia
Cystic Fibrosis
for a fuller list look in the related link below.
# They are SO numerous: Angelman's syndrome, Huntington's Disease, Hemophilia, Turner Syndrome, Tay-Schs disease, sickle cell anemia, Praeder-Willi Syndrome, neurofibromatosis, Klinefelter syndrome, phenylketonuria, Down's Syndrome, Cystic Fibrosis, celiac disease, color blindness, cri du chat, Canavan disease, Duchenne muscular distrophy, Charcot-Marie Tooth Disease, 22q11.2 deletion syndrome, achondroplasia and many, many more.
Having a sibling with Down syndrome does not directly increase the chances of giving birth to a child with Down syndrome. The risk is influenced by maternal age, not family history. If both parents are carriers of the genetic translocation for Down syndrome, the risk may be higher.
Two genetic disorders are Turner's syndrome and cystic fibrosis.
Karyotypes can reveal chromosomal abnormalities associated with genetic diseases, such as Down syndrome or Turner syndrome. By examining the number, size, and structure of chromosomes in a karyotype, geneticists can identify genetic disorders caused by changes in chromosome number or structure. Karyotyping is an important tool in diagnosing and understanding genetic diseases.
Down syndrome is the genetic disorder characterized by varying degrees of mental retardation. It is caused by the presence of an extra copy of chromosome 21. Symptoms of Down syndrome can vary widely, but intellectual disability is a common characteristic.
Docks do not get down syndrome. You have not studied the genetic diseases of ducks to any extent. But one can be sure that ducks too must be getting as many genetic diseases.
albinism. huntington's disease. color blindness. down's syndrome.
A genetic disorder (or a hereditary disease/inherited disorder) is when a wrong gene or chromosomal aberration changes what your genome normally would be. For example: Down's Syndrome or Trisomy 21 which means that that person has 3 copies of chromosome 21 instead of the normal 2.
is down syndrome acquired genetic disease
Down syndrome is a genetic abnormality and would be called a genetic disorder; however, complications associated with Down syndrome can increase the risk of a number of diseases, such as congenital heart disease. To give another example, cancer is a disease, but in some it may stem from a genetic disorder.
Various arthritic conditions and several genetic and neuromuscular diseases, such as Down syndrome and Marfan syndrome, cause muscle imbalances that can create bunions from displacement of the first metatarsal and big toe.
down syndrome
There's many different genetic disorders such as: Down Syndrom Canavan Disease Muenke Syndrome Bloom Syndrome etc
The genetic developmental defect is spelled "Down Syndrome" or sometimes "Down's Syndrome."
# They are SO numerous: Angelman's syndrome, Huntington's Disease, Hemophilia, Turner Syndrome, Tay-Schs disease, sickle cell anemia, Praeder-Willi Syndrome, neurofibromatosis, Klinefelter syndrome, phenylketonuria, Down's Syndrome, Cystic Fibrosis, celiac disease, color blindness, cri du chat, Canavan disease, Duchenne muscular distrophy, Charcot-Marie Tooth Disease, 22q11.2 deletion syndrome, achondroplasia and many, many more.
No, Down's syndrome is only a human genetic disorder. Those with the disorder have an extra chromosome. Raccoons do not get this particular genetic disorder.
That is hard to say because the frequency of Down syndrome if a function of maternal age so it is not fixed. A mom between 20 and 24 years old has a 1/ 1400 risk of having a child with Down syndrome. A mom who is 45 or older has a 1/25 risk. Overall, it is fair to say Down syndrome is one of the most common and best known genetic disease. Other genetic disease such as Cystic Fibrosis, hemochromatosis are also common. The frequency of all these things varies in different populations as well as age. So the question is quite hard to answer without isolating a specific population.