Ankyloblepharon - ectodermal defects - cleft lip or palate (Q83072)
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Ankyloblepharon - ectodermal defects - cleft lip/palate syndrome, designated as Hay Wells syndrome, is characterised by congenital ectodermal dysplasia with wiry, sparse hair; dystrophic nails; slight hypohidrosis; scalp infections; ankyloblepharon filiform adnatum (apposing eyelid margins connected by abnormal tissue strands); hypodontia (missing teeth); maxillary hypoplasia; and cleft lip/palate.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1008188767 |
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| English | Ankyloblepharon - ectodermal defects - cleft lip or palate |
Ankyloblepharon - ectodermal defects - cleft lip/palate syndrome, designated as Hay Wells syndrome, is characterised by congenital ectodermal dysplasia with wiry, sparse hair; dystrophic nails; slight hypohidrosis; scalp infections; ankyloblepharon filiform adnatum (apposing eyelid margins connected by abnormal tissue strands); hypodontia (missing teeth); maxillary hypoplasia; and cleft lip/palate. |
Statements
CID11:ID_1008188767
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dki-india-ID_1008188767
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Concluído
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13 August 2026
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