Talk:Cat eye syndrome

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Medicine: Genetics / Ophthalmology Low‑importance

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	This article is supported by the Ophthalmology task force.

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Untitled

What's with the quote "From the statistic given in paragraph two I will say this is not a very common disease."? —Preceding unsigned comment added by 137.112.150.230 (talk) 23:30, 23 February 2010 (UTC)[reply]

Thank you for noticing that and commenting. An editor has removed it.--FeralOink (talk) 23:14, 22 December 2017 (UTC)[reply]

Some good information present. I would like to see some more genetic information included. I stopped by OMIM and found the following: 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).^[1] Matthewmazurek (talk) 22:39, 17 April 2009 (UTC)[reply]

diff3r3nt f4cts in diff3r3nt l4ngu4g3s,wikip3di4lost th3 trust of th3 own3r of 4 f4ulty k3ybo4rd. — Preceding unsigned comment added by 176.93.195.205 (talk) 02:01, 15 February 2020 (UTC)[reply]

References

^ http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=115470

[1] ttp://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=115470

[1]