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Juvenile Huntington’s disease and paediatric Huntington’s disease
2020Abstract Juvenile Huntington’s disease (JHD) is rare. It is usually defined as someone having an onset before 21 years. A more accurate description would be juvenile-onset HD. The origins of this definition are obscure but the distinction has been recognized for many years.
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The challenge of juvenile Huntington disease
Neurology, 2013In a cohort of patients with suspected juvenile-onset Huntington disease (HD), we compared HD expansion-positive and -negative cases in order to identify parameters that may allow differentiating between them and may act as a guide to clinicians contemplating genetic testing.We analyzed the clinical and genetic characteristics of 76 juvenile-onset ...
Georgios, Koutsis +3 more
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DNA analysis in juvenile Huntington disease
European Journal of Pediatrics, 1989We report a 6-year-old boy with a positive family history of Huntington disease (HD), who presented with ambiguous neurological and psychiatric symptoms. The suspected diagnosis of HD was confirmed by DNA analysis. This new method is very helpful when the first signs of HD cannot be clearly interpreted.
M, Schömig-Spingler +2 more
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Juvenile onset huntington disease
Archives of Neurology, 2007Hun ting ton dis ease is dis tin guished by the triad of dom i nant in her i tance, choreoathetosis and de men tia. The usual age of on set is in the fourth and fifth de cades, but 3–5% of cases be - gin be fore the 15th year and some even in early child hood.
Kevin Biglan, Ira Shoulson
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2014
In approximately 5% of cases of Huntington’s disease, onset is before 20 years of age, and these cases are defined as juvenile Huntington’s disease (JHD). The clinical and pathologic features of JHD overlap with those of typical adult-onset disease, so it is not a distinct entity.
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In approximately 5% of cases of Huntington’s disease, onset is before 20 years of age, and these cases are defined as juvenile Huntington’s disease (JHD). The clinical and pathologic features of JHD overlap with those of typical adult-onset disease, so it is not a distinct entity.
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MR imaging and spectroscopy in juvenile Huntington disease
Pediatric Radiology, 2004Juvenile Huntington disease manifests differently from adult Huntington disease and has more variability in presentation. We describe a child with cognitive decline and adventitial movements in whom Huntington disease was confirmed with genetic testing.
Mark, Schapiro +4 more
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A03 Juvenile Huntington's disease
Journal of Neurology, Neurosurgery & Psychiatry, 2012Juvenile Huntington's disease is defined as having an onset
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