Cerebrofaciothoracic dysplasia (Q89144): Difference between revisions
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13 August 2026
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Latest revision as of 15:42, 15 August 2026
Cerebro-facio-thoracic dysplasia or Pascual-Castroviejo syndrome type 1 is a rare syndrome characterised by facial dysmorphism (brachycephaly, hypertelorism, broad nasal bridge, large philtrum, triangular-shaped mouth and micrognathia), intellectual deficit and costovertebral abnormalities (short, bifid or fused ribs, bony bridges joining the posterior arches in some ribs, hemi vertebrae). Intellectual deficit is constant but the severity varies and patients also have cerebral abnormalities: cortical atrophy, hypoplasia of the corpus callosum and cerebellar vermis.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_804357902 |
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| English | Cerebrofaciothoracic dysplasia |
Cerebro-facio-thoracic dysplasia or Pascual-Castroviejo syndrome type 1 is a rare syndrome characterised by facial dysmorphism (brachycephaly, hypertelorism, broad nasal bridge, large philtrum, triangular-shaped mouth and micrognathia), intellectual deficit and costovertebral abnormalities (short, bifid or fused ribs, bony bridges joining the posterior arches in some ribs, hemi vertebrae). Intellectual deficit is constant but the severity varies and patients also have cerebral abnormalities: cortical atrophy, hypoplasia of the corpus callosum and cerebellar vermis. |
Statements
CID11:ID_804357902
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dki-india-ID_804357902
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Concluído
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13 August 2026
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