File:Nail patella syndrome 01.jpg: Difference between revisions
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:'''Links:''' [[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] | :'''Links:''' [[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] | ||
===Reference=== | ===Reference=== | ||
<pubmed> | <pubmed>22145064</pubmed>| [http://www.panafrican-med-journal.com/content/article/9/31/full Pan Afr Med J.] | ||
====Copyright==== | ====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. | © 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. | ||
Revision as of 15:35, 27 August 2014
Nail Patella Syndrome
(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.
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.
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