Myelin Projekt Deutschland e.V. Assigned diseases:
In the following you will find the diseases that this support group organisation focuses on:
4H leukodystrophy
Adrenomyeloneuropathy
Adult Krabbe disease
Adult-onset autosomal dominant leukodystrophy
Aicardi-Goutières syndrome
Alexander disease
Alexander disease type I
Alexander disease type II
Allan-Herndon-Dudley syndrome
CACH syndrome
CADDS
Canavan disease
Cerebrotendinous xanthomatosis
Congenital or early infantile CACH syndrome
Cree leukoencephalopathy
Cystic leukoencephalopathy without megalencephaly
Early myoclonic encephalopathy
Hereditary diffuse leukoencephalopathy with axonal spheroids and pigmented glia
Hypomyelination with atrophy of basal ganglia and cerebellum
Hypomyelination with brain stem and spinal cord involvement and leg spasticity
Hypomyelination-congenital cataract syndrome
Infantile Krabbe disease
Infantile Refsum disease
Juvenile or adult CACH syndrome
Krabbe disease
Late infantile CACH syndrome
Late-infantile/juvenile Krabbe disease
Leukodystrophy
Leukoencephalopathy with bilateral anterior temporal lobe cysts
Leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome
Leukoencephalopathy with mild cerebellar ataxia and white matter edema
Leukoencephalopathy-dystonia-motor neuropathy syndrome
Leukoencephalopathy-thalamus and brainstem anomalies-high lactate syndrome
Megalencephalic leukoencephalopathy with subcortical cysts
Metachromatic leukodystrophy
Metachromatic leukodystrophy, adult form
Metachromatic leukodystrophy, juvenile form
Metachromatic leukodystrophy, late infantile form
Mild Canavan disease
Nasu-Hakola disease
Neonatal adrenoleukodystrophy
Null syndrome
Ovarioleukodystrophy
Pelizaeus-Merzbacher disease
Pelizaeus-Merzbacher disease in female carriers
Pelizaeus-Merzbacher disease, classic form
Pelizaeus-Merzbacher disease, connatal form
Pelizaeus-Merzbacher disease, transitional form
Pelizaeus-Merzbacher-like disease
Pelizaeus-Merzbacher-like disease due to AIMP1 mutation
Pelizaeus-Merzbacher-like disease due to GJC2 mutation
Pelizaeus-Merzbacher-like disease due to HSPD1 mutation
Peripheral demyelinating neuropathy-central dysmyelinating leukodystrophy-Waardenburg syndrome-Hirschsprung disease
Peroxisome biogenesis disorder
Progressive cavitating leukoencephalopathy
Ravine syndrome
Refsum disease
Severe Canavan disease
Spastic paraplegia type 2
Unknown leukodystrophy
X-linked adrenoleukodystrophy
X-linked cerebral adrenoleukodystrophy
Zellweger syndrome