Authors describe clinical features, CT scan and MRI findings of 4 Egyptian boys (3 brothers
from one sibship and a sporadic case) with Hallervorden-Spatz syndrome (HSS). These …

The Hallervorden-Spatz syndrome (HSS) is a rare condition characterized by extrapyramidal
and pyramidal signs, dystonia, dysarthria, retinal degeneration, dementia and a progressive …

Hallervorden-Spatz syndrome is a rare autosomal recessive disorder that involves
progressive extrapyramidal manifestations. Classical and atypical clinical presentations are …

Hallervorden-Spatz syndrome (HSS) is a rare autosomal recessive neurodegenerative
disorder of childhood. Thirteen patients with this syndrome seen over a period of 7 years …

Hallervorden-Spatz syndrome is a rare neurodegenerative disease of autosomal recessive
inheritance which presents in childhood or early adulthood with dystonia, dysarthria, rigidity …

Hallervorden-Spatz syndrome is generally considered to be an autosomal recessively
hereditary disorder of unknown etiology. Some reported cases have been known to be …

We reported four cases of Hallervorden–Spatz disease. All four siblings (three males and
one female) in the family are affected. The first symptoms of the disease were spastic …

Background The manifestations of the Hallervorden-Spatz disease (HSD) usually appear
during childhood or in adults. They are not specific and magnetic resonance imaging (MRI) …

We report a 20-year-old female with Hallervorden-Spatz syndrome (HSS). This patient is the
product of consanguineous parents. She developed genu valgum, tendency to fall and …

Hallervorden Spatz syndrome (HSS), described in 1.922, is a rare progressive disorder
recessively inherited involving the basal ganglia. It is manifested clinically by mental …