| Literature DB >> 21597311 |
Sabri Aydin1, Bashar Abuzayed, Figen Varlibas, Hulya Apaydin, Murat Mengi, Baris Kucukyuruk, Hakan Hanimoglu, Selin Yagci, Osman Kizilkilic, Murat Hanci.
Abstract
A 23-year-old woman with the medical history of homocystinuria that had been diagnosed at the age of 14 has been non-responsive to treatment. The patient presented with the symptoms of dysphonia, dysarthria and severe dystonia of the neck and left extremities. Blood and urine biochemistry revealed high levels of homocystine. Brain magnetic resonance imaging was normal with no detectable pathologies. Medical treatment strategies were used and repeated injections of botulinum toxin A were administered, but the symptoms showed no significant improvement. The patient was then operated, and deep brain stimulators targeting the bilateral globus pallidus internus were implanted. After the activation of the electrodes, dystonia symptoms showed a remarkable improvement. Good outcome was documented during the follow-up period of 7 months. To our best knowledge, this is the first reported case of homocystinuria-related dystonia symptoms that were successfully treated with deep brain stimulation.Entities:
Mesh:
Year: 2011 PMID: 21597311 DOI: 10.1159/000325703
Source DB: PubMed Journal: Stereotact Funct Neurosurg ISSN: 1011-6125 Impact factor: 1.875