File:Autosomal dominant inheritance.jpg: Difference between revisions

From Embryology
mNo edit summary
 
(3 intermediate revisions by the same user not shown)
Line 3: Line 3:
In this example, a man with an autosomal dominant disorder has two affected children and two unaffected children.
In this example, a man with an autosomal dominant disorder has two affected children and two unaffected children.


Autosomal Dominant Disease
===Examples of Autosomal Dominant Disease===
* Huntington’s Disease (HD) - neurodegenerative disorder characterised by progressive motor abnormality and cognitive deterioration. (More? [[2011_Group_Project_4|Student Project]])


* Autosomal Dominant Polycystic Kidney Disease (ADPKD) - late-onset multisystem disorder characterized by bilateral renal cysts, liver cysts, and an increased risk of intracranial aneurysms. (heterozygous pathogenic variant in PKD1, PKD2, GANAB, or DNAJB11)
* '''Huntington’s Disease''' (HD) - neurodegenerative disorder characterised by progressive motor abnormality and cognitive deterioration. (More? [[2011_Group_Project_4|Student Project]] | {{neural}})
 
 
* '''Autosomal Dominant Polycystic Kidney Disease''' (ADPKD) - late-onset multisystem disorder characterized by bilateral renal cysts, liver cysts, and an increased risk of intracranial aneurysms. (heterozygous pathogenic variant in PKD1, PKD2, GANAB, or DNAJB11) (More? {{Renal}})




Line 13: Line 15:


'''Links:''' {{spermatozoa}} | {{oocyte}} | [http://www.ncbi.nlm.nih.gov/sites/entrez?db=pubmed&cmd=search&term=autosomal_inheritance Search Pubmed - autosomal inheritance]
'''Links:''' {{spermatozoa}} | {{oocyte}} | [http://www.ncbi.nlm.nih.gov/sites/entrez?db=pubmed&cmd=search&term=autosomal_inheritance Search Pubmed - autosomal inheritance]


===Reference===
===Reference===

Latest revision as of 10:59, 23 July 2018

Autosomal dominant inheritance

In this example, a man with an autosomal dominant disorder has two affected children and two unaffected children.

Examples of Autosomal Dominant Disease

  • Huntington’s Disease (HD) - neurodegenerative disorder characterised by progressive motor abnormality and cognitive deterioration. (More? Student Project | neural)


  • Autosomal Dominant Polycystic Kidney Disease (ADPKD) - late-onset multisystem disorder characterized by bilateral renal cysts, liver cysts, and an increased risk of intracranial aneurysms. (heterozygous pathogenic variant in PKD1, PKD2, GANAB, or DNAJB11) (More? renal)


Inheritance Pattern images: Genetic Abnormalities | autosomal dominant | autosomal recessive | X-linked dominant (affected father) | X-Linked dominant (affected mother) | X-Linked recessive (affected father) | X-Linked recessive (carrier mother) | mitochondrial inheritance | Codominant inheritance | Genogram symbols | Genetics

Links: spermatozoa | oocyte | Search Pubmed - autosomal inheritance

Reference

Genetics Home Reference. http://ghr.nlm.nih.gov/handbook/illustrations/autodominant

Copyright

Government information at NLM Web sites is in the public domain. Public domain information may be freely distributed and copied, but it is requested that in any subsequent use the National Library of Medicine (NLM) be given appropriate acknowledgement. http://www.nlm.nih.gov/copyright.html


Cite this page: Hill, M.A. (2024, April 18) Embryology Autosomal dominant inheritance.jpg. Retrieved from https://embryology.med.unsw.edu.au/embryology/index.php/File:Autosomal_dominant_inheritance.jpg

What Links Here?
© Dr Mark Hill 2024, UNSW Embryology ISBN: 978 0 7334 2609 4 - UNSW CRICOS Provider Code No. 00098G

File history

Click on a date/time to view the file as it appeared at that time.

Date/TimeThumbnailDimensionsUserComment
current09:40, 12 May 2010Thumbnail for version as of 09:40, 12 May 2010307 × 396 (64 KB)S8600021 (talk | contribs)Autosomal dominant inheritance In this example, a man with an autosomal dominant disorder has two affected children and two unaffected children. Source: Genetics Home Reference. http://ghr.nlm.nih.gov/handbook/illustrations/autodominant Government info