In genetics, autosomal dominance means that an individual only needs to inherit one allele for a trait in order for that trait to be expressed. An individual must inherit a recessive trait from both parents in order for a recessive trait to be expressed.
These websites will probably explain it better then I can:
http://www.britannica.com/EBchecked/topic/228874/human-genetic-disease/242824/Autosomal-dominant-inheritance
http://www.wrongdiagnosis.com/genetics/dominant.htm
http://www.gig.org.uk/images/gen-dominant.gif
Autosomal dominant inheritance requires that only one copy of a gene pair be defective in order to develop the disorder. Each offspring of a parent with an autosomal dominant disorder has a 50% risk of inheriting the gene
Autosomal dominant is one of several ways that a trait or disorder can be passed down through families.
If a disease is autosomal dominant, it means you only need to get the abnormal gene from one parent in order for you to inherit the disease. One of the parents may often have the disease.
Alternative NamesInheritance - autosomal dominant; Genetics - autosomal dominant
InformationInheriting a disease, condition, or trait depends on the type of chromosome affected (autosomal or sex chromosome). It also depends on whether the trait is dominant or recessive.
A single, abnormal gene on one of the first 22 nonsex chromosomes from either parent can cause an autosomal disorder.
Dominant inheritance means an abnormal gene from one parent is capable of causing disease, even though the matching gene from the other parent is normal. The abnormal gene "dominates" the pair of genes. If just one parent has a dominant gene defect, each child has a 50% chance of inheriting the disorder.
For example, if four children are born to a couple and one parent has an abnormal gene for a dominant disease, statistically two children will inherit the abnormal gene and two children will not. Children who do not inherit the abnormal gene will not develop or pass on the disease.
If someone has an abnormal gene that is inherited in an autosomal dominant manner, then the parents should also be tested for the abnormal gene.
Examples of autosomal dominant disorders include Huntington's disease and neurofibromatosis-1.
See also:
Korf BR. Principles of Genetics. In: Goldman L, Ausiello D, eds. Cecil Medicine. 23rd ed. Philadelphia, Pa: Saunders Elsevier; 2007:chap 37.
Autosomal dominant is one of several ways that a trait or disorder can be passed down through families.
If a disease is autosomal dominant, it means you only need to get the abnormal gene from one parent in order for you to inherit the disease. One of the parents may often have the disease.
Alternative NamesInheritance - autosomal dominant; Genetics - autosomal dominant
InformationInheriting a disease, condition, or trait depends on the type of chromosome affected (autosomal or sex chromosome). It also depends on whether the trait is dominant or recessive.
A single, abnormal gene on one of the first 22 nonsex chromosomes from either parent can cause an autosomal disorder.
Dominant inheritance means an abnormal gene from one parent is capable of causing disease, even though the matching gene from the other parent is normal. The abnormal gene "dominates" the pair of genes. If just one parent has a dominant gene defect, each child has a 50% chance of inheriting the disorder.
For example, if four children are born to a couple and one parent has an abnormal gene for a dominant disease, statistically two children will inherit the abnormal gene and two children will not. Children who do not inherit the abnormal gene will not develop or pass on the disease.
If someone has an abnormal gene that is inherited in an autosomal dominant manner, then the parents should also be tested for the abnormal gene.
Examples of autosomal dominant disorders include Huntington's disease and neurofibromatosis-1.
See also:
Korf BR. Principles of Genetics. In: Goldman L, Ausiello D, eds. Cecil Medicine. 23rd ed. Philadelphia, Pa: Saunders Elsevier; 2007:chap 37.
Reviewed ByReview Date: 04/26/2010
Neil K. Kaneshiro, MD, MHA, Clinical Assistant Professor of Pediatrics, University of Washington School of Medicine. Also reviewed by David Zieve, MD, MHA, Medical Director, A.D.A.M., Inc.
Two copies of an altered gene located on one of the autosomes must be present for an individual to be affected with the trait or condition determined by that gene.
it could be the sickle cells that bring the chromosomal
autosomal dominant
Progeria is autosomal dominant.
No, it is autosomal dominant.
Autosomal dominant allele
Huntingdons chorea is caused by a dominant allele.
When the gene is dominant and the traits are autosomal.
autosomal dominant
Huntington's Disease is an Autosomal Dominant Trait, meaning that only one parent needs to pass the disease for the offspring to inherit it.
Autosomal dominant
There is two answers, it is autosomal dominant showing incomplete dominace
autosomal dominant
Progeria is autosomal dominant.
No, it is autosomal dominant.
It is an autosomal recessive trait.
Autosomal dominant, Autosomal recessive, X-linked recessive and X-linked dominant
Tay-sachs is autosomal.
glaucoma is inherited in an autosomal dominantpattern.which is dominant.