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Czeizel syndrome

From Wikipedia, the free encyclopedia

Czeizel syndrome, also known as Lethal omphalocele-cleft palate syndrome, is a rare dysmorphic syndrome characterized by a cleft lip, a bifid uvula, bilateral talipes equinovarus, bicornuate uterus, and Hydrocephalus internus.[1]

Symptoms

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Usually, Czeizel Syndrome is seen during pregnancy and as a newborn.[1]

References

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  1. ^ a b "Lethal omphalocele-cleft palate syndrome – About the Disease – Genetic and Rare Diseases Information Center". rarediseases.info.nih.gov. Retrieved 2024-03-09.