CECR - cat eye syndrome chromosome region Gene
Also Known as CES
Species: Homo sapiens
About CECR
Summary
Cat eye syndrome (CES) is characterized clinically by the combination of coloboma of the iris and anal atresia with fistula, downslanting palpebral fissures, preauricular tags and/or pits, frequent occurrence of heart and renal malformations, and normal or near-normal mental development. A small supernumerary chromosome (smaller than chromosome 21) is present, frequently has 2 centromeres, is bisatellited, and represents an inv dup(22)(q11).[supplied by OMIM, Aug 2009]
Related Diseases
| Diseases | Alias | |
|---|---|---|
| Cat Eye Syndrome |
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