Table 1.
Phenotypes | Onset | Symptoms | Japanese Patients (At Ddiagnosis by Gifu Univ.) |
---|---|---|---|
Childhood cerebral ALD (CCALD) |
3–10 years | personality and behavioral changes, decreased vision and hearing, impaired intelligence, gait disturbance | 99 |
Adolescent cerebral ALD (AdolCALD) |
11–21 years | similar to CCALD but tends to progress more slowly. | 12 |
Adult cerebral ALD (ACALD) |
after adulthood | personality changes, intellectual deterioration, psychiatric symptoms | 17 |
Adrenomyeloneuropathy (AMN) |
after puberty | gait disturbance, incontinence, impotence, progresses slowly. Some patients may develop cerebral ALD. |
55 |
Olivo-ponto-cerebellar type of ALD (OPCALD) |
after adulthood | cerebellar ataxia, spasticity of the lower limbs, similar to spinocerebellar degeneration. Some patients may develop cerebral ALD. |
6 |
Addison only | after infancy | lethargy, anorexia, weight loss, skin pigmentation Some patients may progress to cerebral ALD or AMN. |
29 |
Presymptomatic | We cannot predict phenotypes and prognosis before onset. | 43 |