Autosomal Dominant Disorders: Difference between revisions

From The School of Biomedical Sciences Wiki
Jump to navigation Jump to search
110103363 (talk | contribs)
No edit summary
Nnjm2 (talk | contribs)
No edit summary
 
(5 intermediate revisions by 2 users not shown)
Line 1: Line 1:
An [https://bms.ncl.ac.uk/wiki/index.php/Autosome autosomal] [[Dominant|dominant]] disorder is a genetically inheritable&nbsp;disorder which the offspring of the affected individuals will show the [[Phenotype|phenotype]] of the disorder whether they are [[Homozygous|homozygous]] dominant or [[Heterozygous|heterozygous]]. In this kind of disorder, the dominant allele carries the defect while the recessive allele is the normal allele and the dominance relationship results in the individual to show the observable defect.<br>
An [[autosomal|autosomal]] [[Dominant|dominant]] disorder is a genetic disorder which the inherited offspring of the affected individuals will show the [[Phenotype|phenotype]] of the disorder whether they are [[Homozygous|homozygous]] dominant or [[Heterozygous|heterozygous]]. In this kind of disorder, the dominant allele carries the defect while the recessive allele is the normal allele and the dominance relationship results in the individual to show the observable defect.<br>  


The pedigree analysis for this particular disorder shows the phenotype of the defect in each generation due to the dominance relationship with equal chances of passing the defect to both males and females offspring.
The [[Pedigree]]&nbsp;analysis&nbsp;for this particular disorder shows the phenotype of the defect in each generation due to the dominance relationship with equal chances of passing the defect to both males and females offspring.  


Example of autosomal dominant disorders are Pseudoachondroplasia, Huntington disease, Polydactyly and etc.
Examples of autosomal dominant disorder are [[Pseudoachondroplasia|Pseudoachondroplasia]], [[Huntington disease|Huntington&nbsp;disease]], Polydactyly and etc.<ref>Griffths A. J. F., Wessler S. R., Lewontin R. C., Carroll S. B. (2008) Introduction to Genetic Analysis. 9th Edition. New York: W. H. Freeman and Company</ref>
 
=== References ===
 
<references />

Latest revision as of 01:30, 1 December 2013

An autosomal dominant disorder is a genetic disorder which the inherited offspring of the affected individuals will show the phenotype of the disorder whether they are homozygous dominant or heterozygous. In this kind of disorder, the dominant allele carries the defect while the recessive allele is the normal allele and the dominance relationship results in the individual to show the observable defect.

The Pedigree analysis for this particular disorder shows the phenotype of the defect in each generation due to the dominance relationship with equal chances of passing the defect to both males and females offspring.

Examples of autosomal dominant disorder are Pseudoachondroplasia, Huntington disease, Polydactyly and etc.[1]

References

  1. Griffths A. J. F., Wessler S. R., Lewontin R. C., Carroll S. B. (2008) Introduction to Genetic Analysis. 9th Edition. New York: W. H. Freeman and Company