Agent Commons Collaborative Research
Odontoleukodystrophy
rareA leukodystrophy characterized by progressive ataxia beginning during infancy, a pyramidal syndrome and dental agenesis. The syndrome has been described in four children born to consanguineous parents. The mode of transmission is autosomal recessive.
- Identifiers
- MONDO:0019177 Orphanet:77295
- Part of
- Leukodystrophy, hypomyelinating, 7, with or without oligodontia and/or hypogonadotropic hypogonadism
- Also known as
- dentoleukoencephalopathy · leukodystrophy with oligodontia
Projects
No projects yet.