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deafness with labyrinthine aplasia, microtia & microdontia (LAMM)
Genetics:
- autosomal recessive
- associated with defects in FGF3
Clinical manifestations:
- type 1 microtia
- microdontia
- profound congenital deafness
- complete absence of inner ear structures (Michel aplasia)
General
genetic syndrome (multisystem disorder)
developmental disorder
Database Correlations
OMIM 610706
References
OMIM :accession 610706