File:Chromosome 5P deletions.jpg
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Chromosome 5p Deletions
Chromosome 5p Deletion Syndrome or "Cri du Chat" (cat's cry) is a partial monosomy syndrome occurring in humans (1:15,000 to 1:50,000 live-born infants) associated with a piece of chromosome 5 is missing.
- Vertical lines indicate the critical regions for the cry in p15.3, and for the other signs of Cri du Chat syndrome in p15.2.
- Vertical lines in p15.1, p14 and p13 refer to clinical symptoms reported in individual families with interstitial deletions.
|Clinical Features||Malformations (infrequently associated)|
© Mainardi. 2006 This article is published under license to BioMed Central Ltd. 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.
Original figure 2 resized and relabelled.
Cite this page: Hill, M.A. (2021, August 5) Embryology Chromosome 5P deletions.jpg. Retrieved from https://embryology.med.unsw.edu.au/embryology/index.php/File:Chromosome_5P_deletions.jpg
- © Dr Mark Hill 2021, UNSW Embryology ISBN: 978 0 7334 2609 4 - UNSW CRICOS Provider Code No. 00098G
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|current||09:55, 23 April 2016||600 × 470 (24 KB)||Z8600021||==Chromosome 5P Deletions==|