File:Partial Deletion of Short Arms of 5.jpg

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English: This photographic collage depicts the karyotype that would represent the chromosomal configuration known as an autosomal deletion syndrome, which has been given the name, cri-du-chat. In this particular case, the cells in a person with cri-du-chat syndrome contained an abnormal chromosomal complement, which involved the deletion of some of the chromosomal material from the short arms of chromosome 5 (5p-), as indicated by the arrow. Cri-du-chat syndrome was the first recognized syndrome due to a chromosomal deletion, in 1963. Aspects of the syndrome manifest themselves as mental retardation, microcephaly, round face, and a laryngeal anomaly that causes infants to sound like a cat when crying, hence its moniker.
Date
Source https://phil.cdc.gov/Details.aspx?pid=12505
Author CDC/ Dr. Allan Ebbin

This media comes from the Centers for Disease Control and Prevention's Public Health Image Library (PHIL), with identification number #12505.

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This image is a work of the Centers for Disease Control and Prevention, part of the United States Department of Health and Human Services, taken or made as part of an employee's official duties. As a work of the U.S. federal government, the image is in the public domain.

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Date/TimeThumbnailDimensionsUserComment
current19:23, 14 September 2020Thumbnail for version as of 19:23, 14 September 20203,139 × 2,528 (296 KB)wikimediacommons>AntiCompositeNumber{{Information |description ={{en|1=This photographic collage depicts the karyotype that would represent the chromosomal configuration known as an autosomal deletion syndrome, which has been given the name, cri-du-chat. In this particular case, the cells in a person with cri-du-chat syndrome contained an abnormal chromosomal complement, which involved the deletion of some of the chromosomal material from the short arms of chromosome 5 (5p-), as indicated by the arrow. Cri-du-chat syndrome wa...

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