The own research were conducted according to the Good Clinical Practice guidelines and accepted by local Bioethics Committee, all patients agreed in writing to participation and these researches. “
“Guillain–Barré Syndrome (GBS) is an acute immune-mediated peripheral neuropathy with a highly variable clinical course and

outcome [1]. It is currently classified into several subtypes by electrophysiological and pathologic criteria. The two major subtypes are acute inflammatory demyelinating polyneuropathy Depsipeptide price (AIDP) and acute motor axonal neuropathy (AMAN). AIDP is the classic form of GBS and is characterized by demyelination as the main pathological process [2]. AMAN is caused by a heterogeneous group of antibiotics directed against the human gangliosides on the axolemma of motor fibers. Autopsy studies in AMAN patients’ revealed degeneration in motor axons with IgG and complement deposits without demyelination, suggesting that the disorder primarily involves the axonal membrane [3] and [4]. The association of anti-ganglioside antibodies with some clinical features of GBS has been documented in several previous studies. Wilson and Yuki found a strong correlation between some types of anti-ganglioside antibodies

particularly anti-GM1 and the rapid progressive OSBPL9 course of the disease [5]. Furthermore,

this high anti-GM1 tended to be associated with a worse STAT inhibitor disability 6 months after the onset of paralysis [6]. Kusunoki et al. found the presence of antibodies that specifically recognizes a new conformational epitope formed by ganglioside complex in the acute-phase sera of some GBS patients, and they demonstrated that these antibodies were associated with severe GBS requiring mechanical ventilation [7]. The purpose of this study was to determine the frequency of different electrophysiological subtypes of GBS among Egyptian children and their association with anti-ganglioside antibodies and to find a correlation between the presence of theses antibodies and some clinical presentations of GBS. In addition we also assessed the role of antiganglioside antibodies in determining the response to different therapeutic interventions. This prospective cohort study included 47 patients fulfilling international criteria for GBS [8], with inability to walk 10 m independently and within two weeks from the onset of neuropathy. Patients were selected from Pediatric Intensive Care Unit (PICU) of Cairo University Specialized hospital, 9 bed capacity, from the period of January 2010 to September 2012.