ORPHA:139399
Adrenomyeloneuropathy
- Body system
- Inborn errors of metabolism
- Inheritance pattern
- X-linked recessive
- Typical age of onset
- Adult
- Estimated prevalence
- Not documented in Orphadata
- Rarity class
- Not documented in Orphadata
ORPHA:139399 is classified under "Inborn errors of metabolism" in the Orphanet nomenclature.
Common signs
- Peripheral axonal degeneration
- Abnormality of the spinal cord
- Distal sensory impairment
- Abnormal circulating fatty-acid concentration
- Progressive spastic paraparesis
- Distal lower limb muscle weakness