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Thickened earlobes-conductive deafness syndrome
rareThickened earlobes-conductive deafness syndrome is characterized by microtia with thickened ear lobes, micrognathia and conductive hearing loss due to congenital ossicular anomalies. It has been described in two families. The mode of inheritance is autosomal dominant.
- Identifiers
- MONDO:0007504 OMIM:128980Orphanet:2405
- Part of
- Hereditary disease
- Also known as
- Escher Hirt syndrome · Escher-Hirt syndrome
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