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ID#:12505
Description:This photomicrographic 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 contain 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.
High Resolution: Click here for hi-resolution image (7.96 MB)
Content Providers(s):CDC/ Dr. Allan Ebbin
Creation Date:1967
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Copyright Restrictions:None - This image is in the public domain and thus free of any copyright restrictions. As a matter of courtesy we request that the content provider be credited and notified in any public or private usage of this image.

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