huntingtons disorder is a genetic disorder caused by dominant alleles. it has a late on set as symptoms are shown after the age of at least 40
The outcome varies. In some children the disorder evolves into a conduct disorder or a mood disorder. Later in life, oppositional defiant disorder can develop into passive aggressive personality disorder or antisocial personality disorder
dependent personality disorder
Approximately 5-10% of the population worldwide is estimated to have a significant bone disorder. This can vary depending on the specific bone disorder and geographic location.
Approximately 10-15% of individuals diagnosed with major depressive disorder will go on to develop bipolar disorder.
Bob is diagnosed with multiple phobias and dependent personality disorder in the movie "What About Bob."
Autosomal Dominant
Huntingtons disease is a genetic/inherited diesease. It is caused by a faulty allele (a dominant one), which can be inherited by parents. Spontanoius mutations may also occur which would cause the faulty gene and therefore huntingtons disorder.
An autosomal genetic disorder is Huntington's disease.
Because Huntington's is a genetic disorder and it is known what sequence in what region causes the disorder.
by inherited disorder from both or one parent, such as diabetes, cystic fibrosis, parkinsons disease, huntingtons disease etc.
the man has huntingtons disease
Get Lost - Huntingtons album - was created in 1999-01.
There are dozens of diseases caused by a genetic defect. They are known as genetic diseases. Sickle Cell anemia, Hemophilia, Tay-Sachs, Huntingtons Disease- and many others are genetic diseases.
No. While it is a hereditary disease it is not at all a bleeding disorder, nor is it only passed by the mother. It is a degenerative, neuropsychiatric disease that can be passed by either the mother or father. If the parent has it, the child's chance of inheritance is of the faulty gene is 50%.
It can be, especially for the family.
The symptoms of Huntingtons Disease are, mental deterioration and uncontrollable movements; symptoms usually appear in middle ages.
Around 1 in 10,000 people are estimated to develop Huntington's disease, a rare genetic disorder. It is caused by a mutation in the HTT gene on chromosome 4.