[childhood genetic disease, transmitted as an X-linked recessive trait, characterized by diffuse abnormality of cerebral white matter and adrenal atrophy; mental deterioration progresses to dementia, aphasia, apraxia, dysarthria, and loss of vision. ( CSP )]
UMLS (CSP) C0162309 Relation/PAR: adrenal disorder
Adrenal Gland Hypofunction
Genetic Condition
LEUKODYSTROPHY
Sphingolipidoses
PEROXISOMAL DISORDERS
Hereditary Central Nervous System Demyelinating Diseases