ORPHA:79255
GM1 gangliosidosis type 1
Also called Infantile GM1 gangliosidosis, Norman-Landing disease
- Body system
- Bone diseases
- Inheritance pattern
- Autosomal recessive
- Typical age of onset
- Infancy, Neonatal
- Estimated prevalence
- Unknown (Worldwide)
- Rarity class
- Unknown
ORPHA:79255 is classified under "Bone diseases" in the Orphanet nomenclature.
Common signs
- Hearing impairment
- Blindness
- Abnormality of the nervous system
- Abnormality of the skeletal system
- Intellectual disability
- Global developmental delay