Deafness – enamel hypoplasia – nail defects (Q59082): Difference between revisions

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Property / Canonical URI: https://id.who.int/icd/entity/1277620176 / rank
 
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CID11:ID_1277620176
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dki-india-ID_1277620176
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Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank
 
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13 August 2026
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Latest revision as of 06:37, 14 August 2026

This syndrome is characterised by sensorineural hearing loss, generalised enamel hypoplasia of the permanent dentition with normal primary dentition, and nail defects (Beau's lines and leukonychia). Less than 10 patients have been described so far. Transmission is autosomal recessive.
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ID_1277620176
    English
    Deafness – enamel hypoplasia – nail defects
    This syndrome is characterised by sensorineural hearing loss, generalised enamel hypoplasia of the permanent dentition with normal primary dentition, and nail defects (Beau's lines and leukonychia). Less than 10 patients have been described so far. Transmission is autosomal recessive.

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      CID11:ID_1277620176
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      dki-india-ID_1277620176
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      Concluído
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      13 August 2026
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