Spondyloepiphyseal dysplasia, Cantu type (Q88343): Difference between revisions
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dki-india-ID_897226700 | |||||||||||||||
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13 August 2026
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Latest revision as of 14:32, 15 August 2026
Spondyloepiphyseal dysplasia, Cantu type is an extremely rare type of spondyloepiphyseal dysplasia described in about 5 patients to date and characterised by clinical signs including short stature, peculiar facies with blepharophimosis, upward slanted eyes, abundant eyebrows and eyelashes, coarse voice, and short hands and feet (brachymetacarpalia, brachymetatarsalia and brachyphalangia).
| Language | Label | Description | Also known as |
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| default for all languages | ID_897226700 |
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| English | Spondyloepiphyseal dysplasia, Cantu type |
Spondyloepiphyseal dysplasia, Cantu type is an extremely rare type of spondyloepiphyseal dysplasia described in about 5 patients to date and characterised by clinical signs including short stature, peculiar facies with blepharophimosis, upward slanted eyes, abundant eyebrows and eyelashes, coarse voice, and short hands and feet (brachymetacarpalia, brachymetatarsalia and brachyphalangia). |
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CID11:ID_897226700
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dki-india-ID_897226700
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Concluído
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13 August 2026
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