File:Nail patella syndrome 02.jpg: Difference between revisions

From Embryology
mNo edit summary
mNo edit summary
 
(3 intermediate revisions by the same user not shown)
Line 5: Line 5:
:[[Integumentary_System_-_Nail_Development|'''NPS Links''']]:  [[:File:Nail patella syndrome 01.jpg|Image - Abnormal Nails]] | [[:File:Nail patella syndrome 02.jpg|Image - Absent Patella]] | [[Integumentary_System_-_Nail_Development|Nail Development]] | [http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=161200 OMIM - nail-patella syndrome] | [http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=602575 OMIM - LMX1B] | [http://www.ncbi.nlm.nih.gov/pubmed/20301311 GeneReviews]
:[[Integumentary_System_-_Nail_Development|'''NPS Links''']]:  [[:File:Nail patella syndrome 01.jpg|Image - Abnormal Nails]] | [[:File:Nail patella syndrome 02.jpg|Image - Absent Patella]] | [[Integumentary_System_-_Nail_Development|Nail Development]] | [http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=161200 OMIM - nail-patella syndrome] | [http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=602575 OMIM - LMX1B] | [http://www.ncbi.nlm.nih.gov/pubmed/20301311 GeneReviews]


:'''Links:''' [[Musculoskeletal System - Limb Development|Limb Development]] | [[Musculoskeletal System - Limb Abnormalities|Limb Abnormalities]] | [[Musculoskeletal System - Appendicular Skeleton Development|Appendicular Skeleton]] |
===Reference===
===Reference===


Line 13: Line 14:
© Nagendra Boopathy Senguttuvan et al.   The Pan African Medical Journal - ISSN 1937-8688. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
© Nagendra Boopathy Senguttuvan et al.   The Pan African Medical Journal - ISSN 1937-8688. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.


 
{{Footer}}
[[Category:Human]][[Category:Integumentary]] [[Category:Nail]][[Category:Abnormal Human]]
[[Category:Human]][[Category:Limb]] [[Category:Bone]][[Category:Abnormal Development]][[Category:X-ray]]

Latest revision as of 17:13, 23 May 2016

Nail Patella Syndrome - Absent Patella

(NPS) rare (1/50,000) Autosomal dominant disorder characterized by hypoplastic or absent patellae, dystrophic nails, dysplasia of the elbows and iliac horns. Potentially due to mutations in LMX1B, a LIM-homeodomain transcription protein.


NPS Links: Image - Abnormal Nails | Image - Absent Patella | Nail Development | OMIM - nail-patella syndrome | OMIM - LMX1B | GeneReviews
Links: Limb Development | Limb Abnormalities | Appendicular Skeleton |

Reference

<pubmed>22145064</pubmed>| Pan Afr Med J.


Copyright

© Nagendra Boopathy Senguttuvan et al. The Pan African Medical Journal - ISSN 1937-8688. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.


Cite this page: Hill, M.A. (2024, June 24) Embryology Nail patella syndrome 02.jpg. Retrieved from https://embryology.med.unsw.edu.au/embryology/index.php/File:Nail_patella_syndrome_02.jpg

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

File history

Yi efo/eka'e gwa ebo wo le nyangagi wuncin ye kamina wunga tinya nan

GwalagizhiNyangagiDimensionsUserComment
current15:45, 27 August 2014Thumbnail for version as of 15:45, 27 August 2014809 × 525 (51 KB)Z8600021 (talk | contribs)==Nail Patella Syndrome - Abnormal Nails== (NPS) rare (1/50,000) Autosomal dominant disorder characterized by hypoplastic or absent patellae, dystrophic nails, dysplasia of the elbows and iliac horns. Potentially due to mutations in LMX1B, a LIM-homeod...

There are no pages that use this file.

Metadata