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.
47 XXY
XY and XX
Usher syndrome is a relatively rare genetic disorder caused by a mutation. The gene is not carried on one of the sex chromosomes (X or Y).
There are many thousands of different mutations.
A genetic disorder is an abnormal condition that a person inherits through genes or chromosomes. an example is autism. human being
Gene Therapy cannot treat · Phenylketonuria · Gaucher Disease · Lesch-Nyhan Syndrome · Urea Cycle Disorders · Duchenne Muscular Dystrophy
Progeria causes you to have missing chromosomes in your body function
Usher syndrome is a relatively rare genetic disorder caused by a mutation. The gene is not carried on one of the sex chromosomes (X or Y).
Klinefelters is sex chromosome trisomy. Down Syndrome is trisomy. One of the most common forms of MD is sex-linked and affects boys more frequently than it does girls.
Neither. It is an extra #21 chromosome.
It is neither recessive nor dominant because it is a chromosomal disorder and not just a problem present in a single gene.
There are many thousands of different mutations.
Down syndrome is caused by an additional chromosome while PKU is due to a mutation or defect in a gene.
Hungtington's disease is a dominant mutation in the gene that codes for the protein 'Huntington' It only affects a single gene, the remainder of the chromosome is unaffected and therefore it is not a chromosomal abnormality
Yes. Marfan syndrome is caused by a defect (or mutation) in the gene that tells the body how to make fibrillin-1.
Noonan syndrome is caused by the mutation in a particular gene. It is a genetic disorder which means that the child which is born with this disorder, must have been in their parents.
Usher syndrome is inherited as an autosomal recessive trait. The term autosomal means that the mutated gene is not located on either of the chromosomes that determine a person's sex; in other words, both males and females can have the disorder and can pass along the disorder to a child. The word recessive means that to have Usher syndrome, an individual must receive a mutated form of the Usher syndrome gene from each parent. If a child has a mutation in one Usher syndrome gene but the other gene is normal, he or she is predicted to have normal vision and hearing. Individuals with a mutation in a gene that can cause an autosomal recessive disorder are called carriers, because they "carry" the gene with a mutation but show no symptoms of the disorder. If both parents are carriers of a mutated gene for Usher syndrome, they will have a one-in-four chance of having a child with Usher syndrome with each birth.
It is the result of a chromosomal abnormality, in which there is an extra chromsome on the chromosome 21 pair. This is call trisomy 21.
It is neither recessive nor dominant because it is a chromosomal disorder and not just a problem present in a single gene.