Zechi-Ceide syndrome
| Zechi-Ceide syndrome | |
|---|---|
| Other names | Occipital atretic cephalocele-unusual facies-large feet syndrome |
| Symptoms | facial abnormalities, large feet and mental deficiency |
Zeichi-Ceide syndrome is a rare disease discovered in 2007. It is named after its discoverer, R.M. Zeichi-Ceide, who observed three siblings born of consanguineous parents with distinctive characteristics, including facial anomalies, large feet, mental deficiency, and occipital atretic cephalocele. The investigators suspected the symptoms were caused by autosomal recessive inheritance.[1]
As a rare disease, Zeichi-Ceide syndrome is registered in the Online Mendelian Inheritance in Man[2] and the U.S. National Institutes of Health's Genetic and Rare Diseases databases.[3]
References[edit]
- ^ Zechi-Ceide, Roseli Maria; Guion-Almeida, Maria Leine; Zanchetta, Sthella; Richieri-Costa, Antonio (2007-12-15). "Occipital atretic cephalocele, striking facial anomalies, and large feet in three siblings of a consanguineous union". American Journal of Medical Genetics Part A. 143A (24): 3295–3301. doi:10.1002/ajmg.a.32019. ISSN 1552-4833. PMID 17907157. S2CID 37739230.
- ^ "OMIM Entry - 612916 - ZECHI-CEIDE SYNDROME". www.omim.org. Retrieved 2016-03-01.
- ^ "Zechi Ceide syndrome | Disease | Overview | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program". rarediseases.info.nih.gov. Retrieved 2016-03-01.
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