Oral-facial-digital syndrome type 8 (Q63068): Difference between revisions
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Síndrome oral-facial-digital (OFD), tipo 8 é uma síndrome de malformação caracterizada por lobulação da língua, fenda mediana do lábio superior, ponta nasal larga ou bífida, hipertelorismo ou telecanto, polidactilia pré-axial e pós-axial bilateral, tíbia e/ou rádio anormais, baixa estatura, hipoplasia da epiglote, duplicação dos háluces e déficit intelectual leve. | |||
| description / en | description / en | ||
Oral-facial-digital (OFD) syndrome, type 8 is a malformation syndrome characterised by tongue lobulation, median cleft upper lip, broad or bifid nasal tip, hypertelorism or telecanthus, bilateral preaxial and postaxial polydactyly, abnormal tibiae and/or radii, short stature, hypoplasia of the epiglottis, duplication of the halluces and mild intellectual deficit. | |||
Revision as of 10:33, 14 August 2026
Oral-facial-digital (OFD) syndrome, type 8 is a malformation syndrome characterised by tongue lobulation, median cleft upper lip, broad or bifid nasal tip, hypertelorism or telecanthus, bilateral preaxial and postaxial polydactyly, abnormal tibiae and/or radii, short stature, hypoplasia of the epiglottis, duplication of the halluces and mild intellectual deficit.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1948779753 |
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| English | Oral-facial-digital syndrome type 8 |
Oral-facial-digital (OFD) syndrome, type 8 is a malformation syndrome characterised by tongue lobulation, median cleft upper lip, broad or bifid nasal tip, hypertelorism or telecanthus, bilateral preaxial and postaxial polydactyly, abnormal tibiae and/or radii, short stature, hypoplasia of the epiglottis, duplication of the halluces and mild intellectual deficit. |
