Neuroferritinopathy pedigree in 2 families from India
Objective: The abstract provides description of first case report of two Indian families with Neuroferritinopathy (NFT) pedigree. Background: NFT is a rare autosomal dominant movement disorder caused…Fentanyl Induced Chorea: A Case Report
Objective: To report the acute onset of generalized chorea as an adverse reaction to transdermal fentanyl Background: Chorea can present with degenerative conditions or in an…Three distinct cases of methamphetamine induced movement disorders
Objective: To detail three cases of methamphetamine induced movement disorders with unique clinical phenotypes. Background: MA is an addictive psychostimulant that affects both the central…Children with idiopathic tics reveal additional features of hyperkinetic movement disorders
Objective: To investigate whether children with tics reveal features of additional hyperkinetic movement disorders. Background: The patho-physiology for idiopathic tic disorders is unknown, although underlying…Phenotypic insights into ADCY5-associated disease
Objective: We provide detailed clinical data on seven patients from six new kindreds with mutations in the ADCY5 gene, in order to expand and define…Choreoathetosis associated with cervical dystonia as clinical presentation of thyrotoxicosis: A rare condition
Objective: To describe the first report of Cervical Dystonia and Choreoatetosis associated in the same patient with hyperthyroidism (thyrotoxicosis). Background: Thyroid Disease is related with…Acute movement disorders in Tunisian childhood
Objective: To describe clinical, imaging and therapeutic features in 80 children with acute movement disorders. Background: Acute movement disorders are usually misdiagnosed in childhood. Our…Alternating hemiplegia of childhood: Movement disorders and epilepsy due to mutuations in ATP1A3
Objective: To present 2 cases of children with genetic confirmative test of alternating hemiplejia of childhood. Background: Alternating hemiplegia of childhood (AHC) is a dominant…