OBJECTIVES: To confirm linkage of the locus of the major form of hyperekplexia to markers on chromosome 5q, to screen for a point mutation in the gene encoding the alpha 1 subunit of the glycine receptor, and to investigate whether the putative "minor" form of hyperkeplexia consisting of an excessive startle response without stiffness, is based on the same genetic defect as the major form. DESIGN: A survey of various symptoms of hyperekplexia was performed in the Dutch pedigree. Linkage studies were performed for these symptoms. SETTING: Subjects were visited at home, and the genetic study was performed at University Hospital Leiden, (the Netherlands). PATIENTS: A history was taken from 76 subjects in the pedigree, and neurologic examinatio...
BACKGROUND: Hyperekplexia is a rare but well-delineated clinical syndrome of pathological startl...
Hyperekplexia is a rare, but potentially fatal, neuromotor disorder characterized by exaggerated sta...
Hyperekplexia is characterised by neonatal hypertonia and an exaggerated startle reflex in response ...
Objectives: To confirm linkage of the locus of the major form of hyperekplexia to markers on chromos...
Hyperekplexia (MIM: 149400): or startle disease, is an autosomal dominant neurological disorder char...
Hyperekplexia is a hereditary neurological disorder characterized by excessive startle responses. Wi...
Background: Patients with hereditary hyperekplexia have excessive startle responses that are accompa...
Hyperekplexia is a hereditary neurological disorder characterized by excessive startle responses. Wi...
Background: The major and minor forms of hereditary hyperekplexia (HE) are characterized by excessiv...
Hyperekplexia (MIM 149400), or startle disease, is a neurological disorder characterized by generali...
The major form of familial hyperekplexia, a rare autosomal dominant disorder, is characterized by an...
BACKGROUND: Hyperekplexia is a rare but well-delineated clinical syndrome of pathological startl...
Hyperekplexia is a rare, but potentially fatal, neuromotor disorder characterized by exaggerated sta...
Hyperekplexia is characterised by neonatal hypertonia and an exaggerated startle reflex in response ...
Objectives: To confirm linkage of the locus of the major form of hyperekplexia to markers on chromos...
Hyperekplexia (MIM: 149400): or startle disease, is an autosomal dominant neurological disorder char...
Hyperekplexia is a hereditary neurological disorder characterized by excessive startle responses. Wi...
Background: Patients with hereditary hyperekplexia have excessive startle responses that are accompa...
Hyperekplexia is a hereditary neurological disorder characterized by excessive startle responses. Wi...
Background: The major and minor forms of hereditary hyperekplexia (HE) are characterized by excessiv...
Hyperekplexia (MIM 149400), or startle disease, is a neurological disorder characterized by generali...
The major form of familial hyperekplexia, a rare autosomal dominant disorder, is characterized by an...
BACKGROUND: Hyperekplexia is a rare but well-delineated clinical syndrome of pathological startl...
Hyperekplexia is a rare, but potentially fatal, neuromotor disorder characterized by exaggerated sta...
Hyperekplexia is characterised by neonatal hypertonia and an exaggerated startle reflex in response ...