ORPHA:309282
Alpha-mannosidosis, infantile form
Also called Lysosomal alpha-D-mannosidase deficiency, infantile form
- Body system
- Neurological diseases
- Inheritance pattern
- Autosomal recessive
- Typical age of onset
- Infancy
- Estimated prevalence
- Not documented in Orphadata
- Rarity class
- Not documented in Orphadata
ORPHA:309282 is classified under "Neurological diseases" in the Orphanet nomenclature.
Common signs
- Otitis media
- Delayed speech and language development
- Dysostosis multiplex
- Intellectual disability
- Specific learning disability
- Recurrent infections