Main > Medical terms> Akrotsefalopolisindaktiliya of type I

Akrotsefalopolisindaktiliya of type I

Akrotsefalopolisindaktiliya of type I (acrocephalopolysyndactylia; Greek akros – the most remote, extreme, high + kephale – the head + poly – is a lot of + syn – together + daktylos – a finger; synonym: Noaka a syndrome) – the hereditary disease which is characterized by a syndactylia, a turricephaly and doubling of the increased thumbs of legs. The disease is inherited on autosomal dominantly type.

 
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