X-linked recessive disorder: Difference between revisions

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Cleaned up the text. Cleaned up the references. Not one link!!!! So I added a few. You could add some more.
 
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Some recessive genes are located on the X chromosome and are therefore inherited differently in males and females. For a male, who has one X chromosome, the recessive phenotype is always expressed. For a female, however, the phenotype is only expressed if she is homozygous for the recessive allele. If she is heterozygous, she is simply a carrier of the allele. In 1910, Thomas Hunt Morgan showed in flies that the white-eye mutation was X-linked thanks to crosses and reciprocal crosses<ref name="dl">Daniel L. Hartl and Maryellen Ruvolo, Genetics: Analysis of Genes and Genomes, Eighth edition, USA, Jones and Bartlett Learning, 2012</ref>.  
Some [[recessive genes|recessive genes]] are located on the [[X chromosome|X chromosome]] and are therefore inherited differently in [[males|males]] and [[females|females]]. For a male, who has one X chromosome, the [[recessive phenotype|recessive phenotype]] is always expressed. For a female, however, the [[phenotype|phenotype]] is only expressed if she is [[homozygous|homozygous]] for the recessive allele. If she is [[heterozygous|heterozygous]], she is simply a carrier of the allele. In 1910, [[Thomas Hunt Morgan|Thomas Hunt Morgan]] showed in flies that the white-eye mutation was [[X-linked|X-linked]] thanks to crosses and [[reciprocal crosses|reciprocal crosses]]<ref name="dl">Daniel L. Hartl and Maryellen Ruvolo, Genetics: Analysis of Genes and Genomes, Eighth edition, USA, Jones and Bartlett Learning, 2012</ref>.  


Many diseases follow the same inheritance pattern. These are known as X-linked recessive disorders. <ref name="dl">Daniel L. Hartl and Maryellen Ruvolo, Genetics: Analysis of Genes and Genomes, Eighth edition, USA, Jones and Bartlett Learning, 2012</ref>.  
Many diseases follow the same inheritance pattern. These are known as X-linked recessive disorders<ref name="dl">Daniel L. Hartl and Maryellen Ruvolo, Genetics: Analysis of Genes and Genomes, Eighth edition, USA, Jones and Bartlett Learning, 2012</ref>.  


<u>'''Examples of X-linked recessive disorders:'''</u>
=== Examples of X-linked recessive disorders: ===


*Red-green colour blindness<ref>http://www.color-blindness.com/deuteranopia-red-green-color-blindness/</ref>
==== Red-green colour blindness<ref>http://www.color-blindness.com/deuteranopia-red-green-color-blindness/</ref> ====


Red-green color blindness where a person cannot distinguish shades of red and green. Their visual acuity is normal and there are no serious complications; however, affected individuals may not be considered for certain occupations involving transportation or the Armed Forces where color recognition is required. Males are affected more often than females, because the gene is located on the X chromosome.  
Red-green colour blindness where a person cannot distinguish shades of red and green. Their visual acuity is normal and there are no serious complications; however, affected individuals may not be considered for certain occupations involving transportation or the Armed Forces where colour recognition is required. Males are affected more often than females, because the gene is located on the X chromosome.  


*Haemophilia<ref>https://www.nhs.uk/conditions/haemophilia/</ref>
==== Haemophilia<ref>https://www.nhs.uk/conditions/haemophilia/</ref> ====


Hemophilia is a disorder where the blood cannot clot properly due to a deficiency of a clotting factor called Factor VIII. This results in abnormally heavy bleeding that will not stop, even from a small cut. People with hemophilia bruise easily and can have internal bleeding into their joints and muscles.  
Hemophilia is a disorder where the blood cannot clot properly due to a deficiency of a clotting factor called Factor VIII. This results in abnormally heavy bleeding that will not stop, even from a small cut. People with haemophilia bruise easily and can have internal bleeding into their joints and muscles.  


=== References  ===
=== References  ===


<references />
<references />

Latest revision as of 22:27, 4 December 2017

Some recessive genes are located on the X chromosome and are therefore inherited differently in males and females. For a male, who has one X chromosome, the recessive phenotype is always expressed. For a female, however, the phenotype is only expressed if she is homozygous for the recessive allele. If she is heterozygous, she is simply a carrier of the allele. In 1910, Thomas Hunt Morgan showed in flies that the white-eye mutation was X-linked thanks to crosses and reciprocal crosses[1].

Many diseases follow the same inheritance pattern. These are known as X-linked recessive disorders[1].

Examples of X-linked recessive disorders:

Red-green colour blindness[2]

Red-green colour blindness where a person cannot distinguish shades of red and green. Their visual acuity is normal and there are no serious complications; however, affected individuals may not be considered for certain occupations involving transportation or the Armed Forces where colour recognition is required. Males are affected more often than females, because the gene is located on the X chromosome.

Haemophilia[3]

Hemophilia is a disorder where the blood cannot clot properly due to a deficiency of a clotting factor called Factor VIII. This results in abnormally heavy bleeding that will not stop, even from a small cut. People with haemophilia bruise easily and can have internal bleeding into their joints and muscles.

References

  1. 1.0 1.1 Daniel L. Hartl and Maryellen Ruvolo, Genetics: Analysis of Genes and Genomes, Eighth edition, USA, Jones and Bartlett Learning, 2012
  2. http://www.color-blindness.com/deuteranopia-red-green-color-blindness/
  3. https://www.nhs.uk/conditions/haemophilia/