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Waardenburg synrome is an autosomal genetic disorder characterized by deafness, confluent brows, early grey hair as young as 12, different colored eyes or unusually brilliant blue eyes. Source US NIH Deafness and other communcation disorders. Its named Waardenburg because it was discovered Prietrus Waardenburg who noticed girls and boys with unmatching eyes tend to deafness.
There are four main types.
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Turners syndrome is what type of disorder?
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.
What type of disorder is klinefelters syndrome gene or chromosomal?
Chromosomal, because the person with Klinefelter's would have 47 chromosomes. A genetic disorder would be any disorder having to do with genes, but would not necessarily mean having an extra chromosome.
What type of genetic disorder is muscular dystrophy?
Muscular dystrophy is a genetic disorder that causes progressive weakening and deterioration of the muscles. It results from mutations in genes responsible for the structure and function of muscle fibers. There are several types of muscular dystrophy, each with specific genetic causes and patterns of muscle weakness.
What can too few of a type of chromosome cause?
Too few of a type of chromosome can cause genetic disorders or death. Turner Syndrome occurs when there is a missing X chromosome.
What type of mutation causes bipolar?
Bipolar disorder affects men and women equally and usually appears between the ages of 15 and 25. The exact cause is unknown, but it occurs more often in relatives of people with bipolar disorder.
Turners syndrome is what type of disorder?
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.
Which is a recessive genetic disorder down syndrome type ab blood type o blood cystic fibrosis?
cystic fibrosis
What must be the genetic make-up of a male calico cat and what type of chromosome disorder does this most resemble?
XXY, Klinefilter's syndrome
What type of mutation is tourettes syndrome?
Tourette syndrome is believed to be a complex disorder with a combination of genetic and environmental factors contributing to its development. It is not caused by a single mutation, but rather likely involves several genetic variations that increase susceptibility to the disorder.
What is Usher syndrome?
Usher syndrome is a rare inherited disorder primarily characterized by deafness due to an impaired ability of the auditory nerves to transmit sensory input to the brain(sensorineual hearing loss) accompanied by retinitis pigmentosa, a disorder that causes progressive loss of vision.Researchers have identified three types of Usher syndrome and debated the existence of a fourth type. The age at which the disorder appears along with the severity of symptoms distinguishes the different types of Usher syndrome. Usher syndrome is inherited as an autosomal recessive genetic trait. The possible fourth type of Usher syndrome may be inherited as an X-linked genetic trait.source: WEBMD
Which type of disorder is muscular dystrophy?
Muscular dystrophy is a type of genetic disorder. The disorder weakens the muscles until they can no longer move. People with this disorder do not produce a protein needed for healthy muscles.
What type is the genetic disorder of the diabetes?
Type I diabetes mellitus is the genetic form of the disease.
Is Hunter Syndrome and Huntington's Chorea the same?
No, Hunter Syndrome (also known as Mucopolysaccharidosis type II) is a rare genetic disorder that affects metabolism. It is caused by the lack of an enzyme in the body. On the other hand, Huntington's chorea (also known as Huntington's disease) is a different genetic disorder that affects the brain, leading to movement, cognitive, and psychiatric symptoms. While both are genetic disorders, they affect different systems in the body.
One type of genetic bleeding disorder?
Heamophilia
What type of mutation is marfan syndrome?
Marfan syndrome is a genetic disorder caused by mutations in the fibrillin-1 (FBN1) gene. These mutations can result in abnormalities in connective tissues, leading to symptoms such as tall stature, long limbs, heart defects, and eye problems.
What type of syndrome was J.R.R. Tolkien thought to have?
Post Traumatic Stress Disorder.
What type of disorder is klinefelters syndrome gene or chromosomal?
Chromosomal, because the person with Klinefelter's would have 47 chromosomes. A genetic disorder would be any disorder having to do with genes, but would not necessarily mean having an extra chromosome.
