Filippi syndrome (Q94166): Difference between revisions
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Síndrome de Filippi é uma síndrome genética caracterizada por microcefalia, sindactilia cutânea dos dedos das mãos e dos pés, déficit intelectual, atraso de crescimento e uma fácies característica (ponte nasal alta e larga, asas nasais finas, micrognatia e linha do cabelo frontal alta). | |||
| description / en | description / en | ||
Filippi syndrome is a genetic syndrome characterised by microcephaly, cutaneous syndactyly of the fingers and toes, intellectual deficit, growth retardation and a characteristic facies (high and broad nasal bridge, thin alae nasi, micrognathia and a high frontal hairline). | |||
Revision as of 09:17, 16 August 2026
Filippi syndrome is a genetic syndrome characterised by microcephaly, cutaneous syndactyly of the fingers and toes, intellectual deficit, growth retardation and a characteristic facies (high and broad nasal bridge, thin alae nasi, micrognathia and a high frontal hairline).
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1989471300 |
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| English | Filippi syndrome |
Filippi syndrome is a genetic syndrome characterised by microcephaly, cutaneous syndactyly of the fingers and toes, intellectual deficit, growth retardation and a characteristic facies (high and broad nasal bridge, thin alae nasi, micrognathia and a high frontal hairline). |
