[X-linked recessive abnormality in copper absorption marked by severe cerebral degeneration and arterial changes resulting in death in infancy and by sparse, brittle scalp hair. ( CSP )]
UMLS (CSP) C0022716 Relation/PAR: Hair Diseases
inborn metal metabolism disorder
syndrome
CEREB DEGENERATION NOS
Heredodegenerative Disorders, Nervous System
Brain Diseases, Metabolic, Inborn