Case series of autosomal recessive hereditary spastic paraparesis with novel mutation in SPG 7 gene

From the Department of Neurology (Bhattacharjee), from Plymouth Hospital NHS Trust, Department of Neurology (Bhattacharjee), Plymouth Hospital NHS Trust, from Sheffield Diagnostic Genetics Service (Beauchamp), Sheffield Children’s NHS Foundation Trust, Sheffield, United Kingdom, and from Hermitage Medical Clinic (Murray), Mater University Hospital and Dublin Neurological Institute (Lynch), Dublin, Ireland

From the Department of Neurology (Bhattacharjee), from Plymouth Hospital NHS Trust, Department of Neurology (Bhattacharjee), Plymouth Hospital NHS Trust, from Sheffield Diagnostic Genetics Service (Beauchamp), Sheffield Children’s NHS Foundation Trust, Sheffield, United Kingdom, and from Hermitage Medical Clinic (Murray), Mater University Hospital and Dublin Neurological Institute (Lynch), Dublin, Ireland

From the Department of Neurology (Bhattacharjee), from Plymouth Hospital NHS Trust, Department of Neurology (Bhattacharjee), Plymouth Hospital NHS Trust, from Sheffield Diagnostic Genetics Service (Beauchamp), Sheffield Children’s NHS Foundation Trust, Sheffield, United Kingdom, and from Hermitage Medical Clinic (Murray), Mater University Hospital and Dublin Neurological Institute (Lynch), Dublin, Ireland

From the Department of Neurology (Bhattacharjee), from Plymouth Hospital NHS Trust, Department of Neurology (Bhattacharjee), Plymouth Hospital NHS Trust, from Sheffield Diagnostic Genetics Service (Beauchamp), Sheffield Children’s NHS Foundation Trust, Sheffield, United Kingdom, and from Hermitage Medical Clinic (Murray), Mater University Hospital and Dublin Neurological Institute (Lynch), Dublin, Ireland