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1.
Cell Transplant ; 21 Suppl 1: S79-90, 2012.
Artigo em Inglês | MEDLINE | ID: mdl-22507683

RESUMO

Neurological disorders such as muscular dystrophy, cerebral palsy, and injury to the brain and spine currently have no known definitive treatments or cures. A study was carried out on 71 children suffering from such incurable neurological disorders and injury. They were intrathecally and intramuscularly administered autologous bone marrow-derived mononuclear cells. Assessment after transplantation showed neurological improvements in muscle power and a shift on assessment scales such as FIM and Brooke and Vignos scale. Further, imaging and electrophysiological studies also showed significant changes in selective cases. On an average follow-up of 15 ± 1 months, overall 97% muscular dystrophy cases showed subjective and functional improvement, with 2 of them also showing changes on MRI and 3 on EMG. One hundred percent of the spinal cord injury cases showed improvement with respect to muscle strength, urine control, spasticity, etc. Eighty-five percent of cases of cerebral palsy cases showed improvements, out of which 75% reported improvement in muscle tone and 50% in speech among other symptoms. Eighty-eight percent of cases of other incurable neurological disorders such as autism, Retts Syndrome, giant axonal neuropathy, etc., also showed improvement. No significant adverse events were noted. The results show that this treatment is safe, efficacious, and also improves the quality of life of children with incurable neurological disorders and injury.


Assuntos
Células da Medula Óssea/citologia , Transplante de Medula Óssea/métodos , Doenças do Sistema Nervoso/cirurgia , Transplante de Células-Tronco/métodos , Criança , Pré-Escolar , Humanos , Imageamento por Ressonância Magnética , Qualidade de Vida , Transplante Autólogo
3.
Indian J Med Sci ; 64(1): 41-4, 2010 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-22301809

RESUMO

Giant axonal neuropathy is a rare disorder of autosomal recessive inheritance, morphologically characterized by accumulation of neurofilaments in enlargements of preterminal regions of central and peripheral axons. We present a 7-year-old girl with thick and tightly curled lackluster hair suffering from giant axonal neuropathy. The diagnosis was confirmed on the brain MRI which showed white matter abnormalities in the anterior and posterior periventricular regions as well as the cerebellar white matter. In view of the same, the patient was given intrathecal autologous bone marrow-derived stem cell therapy as part of the neuroregenerative rehabilitation therapy protocol. The patient showed functional improvements in her disability after receiving the therapy. A detailed case report is presented here with.


Assuntos
Neuropatia Axonal Gigante/diagnóstico , Neuropatia Axonal Gigante/cirurgia , Transplante de Células-Tronco Hematopoéticas/métodos , Imageamento por Ressonância Magnética/métodos , Células da Medula Óssea , Criança , Feminino , Seguimentos , Neuropatia Axonal Gigante/genética , Humanos , Injeções Espinhais , Doenças Raras , Recuperação de Função Fisiológica , Medição de Risco , Índice de Gravidade de Doença , Transplante Autólogo , Resultado do Tratamento
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