Copyright: © 2008 Elsevier Ltd. Published by Elsevier Ltd. Hereditary spastic paraplegia (HSP) describes a heterogeneous group of genetic neurodegenerative disorders ...

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Copyright: © 2008 Elsevier Ltd. Published by Elsevier Ltd. Hereditary spastic paraplegia (HSP) describes a heterogeneous group of genetic neurodegenerative disorders ...

kliinikum.ee Background Hereditary spastic paraplegia (HSP) comprises a group of rare neurodegenerative disorders characterised by progressive spasticity and hyperreflexia of the legs. Neurogenic ...

We had every gene in her body mapped, and at 14 months old, Tallulah was officially diagnosed with Hereditary Spastic Paraplegia Type 56 (SPG56) - an incurable brain disease so rare no one else in ...

Hereditary spastic paraplegia (HSP) is a very rare disorder with myriad of underlying genetic abnormalities. However, imaging can show typical findings regardless of underlying mutation. ‘Ear of the ...

Diagnosing hereditary spastic paraplegia (HSP) in paediatric patients can be challenging, especially when there is no positive family history. Children are often initially misdiagnosed with cerebral ...

We describe a family with pure X-linked hereditary spastic paraplegia (HSP) and report linkage to X-chromosome DNA probes. A 6-generation pedigree (K313) with 12 affected males is presented.

You will be able to get a quick price and instant permission to reuse the content in many different ways. Hereditary spastic paraparesis (HSP) or the Strümpell-Lorrain syndrome is the name given to a ...

At 12 years, the patient was a wheelchair user with spastic paraplegia of lower limbs, discrete signs of ataxia (dysmetria, slowed speech and nystagmus) and pale optic discs. He complained of dryness ...