Hallervorden-Spatz Syndrome

Hallervorden-Spatz syndrome
medical dictionary
A progressive hereditary disorder with marked reduction in the number of myelin sheaths of the globus pallidus and substantia nigra with accumulation of iron pigment.

Hallervorden-Spatz Syndrome
HSS
Pantothenate Kinase Associated Neurodegeneration (PKAN)
Pigmentary Degeneration of Globus Pallidus, Substantia Nigra, Red Nucleus
NBIA1 ...

Hallervorden-Spatz Syndrome ... Dysarthria
Hashimoto's Thyroiditis ... hoarse voice
Heidenhain syndrome ... dysarthria
Heller-Nelson syndrome ... high-pitched voice
Hemiplegic migraine, familial type 2 ... aphasia ...

Hallervorden-Spatz Syndrome
Hallopeau I Disease
Hallopeau's Disease, Type I
Hallux Duplication, Postaxial Polydactyly, and Absence of Corpus Callosum
HAM/TSP
Hamartoma of the Lymphatics
Hamman-Rich Syndrome ...

Hallervorden-Spatz syndrome see Neuroacanthocytosis disorders
Harlequin Ichthyosis see Ichthyosis
Hashimoto's disease see Thyroid disorders
Hashimoto's Encephalitis
Hashimoto's Encephalopathy see Hashimoto's Encephalitis
HCH see Hypochondroplasia ...

Dalf, Dentate Cerebellar Ataxias, Diagnostic Technic, Urologic, Drug Approval, New, Duramorph, Ejection Seat, Glycoprotein, Glycyl T RNA Synthetase, Goretex, Hallervorden-Spatz Syndrome, Health Care Industry, HLA A DNA Probes, HLA DR6 Antigen, ...

Pantothenate kinase-associated neurodegeneration (formerly called Hallervorden-Spatz syndrome) is a disorder of the nervous system. This condition is characterized by progressive difficulty with movement, typically beginning in childhood.

parkinsonism that accompanies other neurological conditions - such as Shy-Drager syndrome (multiple system atrophy), progressive supranuclear palsy, Wilson's disease, Huntington's disease, Hallervorden-Spatz syndrome, Alzheimer's disease, ...

See also: Symptom, Deficiency, Dystrophy, Dementia, Poisoning