ACTRN12605000128695
Recruiting
未知
Improved characterisation of the clinical phenotype of Hereditary Motor Sensory Neuropathy of neuronal type with onset of symptoms in early childhood, especially with respect to disease progression with age and the incidence of such complications as foot deformity, contractures, scoliosis and respiratory involvement - an observational study.
The Children's Hospital at Westmead0 sites20 target enrollmentAugust 11, 2005
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Hereditary motor sensory neuropathy of neuronal type with onset in early childhood
- Sponsor
- The Children's Hospital at Westmead
- Enrollment
- 20
- Status
- Recruiting
- Last Updated
- 6 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Subjects will have a diagnosis of HMSN of neuronal type with onset in early childhood, based upon their clinical findings and family history, neurophysiological assessments and, where applicable, pathological testing (nerve and muscle biopsies).
Exclusion Criteria
- •No exclusion criteria
Outcomes
Primary Outcomes
Not specified
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