Özet:

Aim: Guillain Barre Syndrome (GBS) is an acute inflammatory polyneuropathy characterized by rapidly progressive, ascending, symmetric weakness and areflexia. It is the most common cause of acute flask paralysis in childhood. It is frequently characterized by progressive weakness, associated mild sensory symptoms, and albuminocytologic dissociation that often occur several days or weeks after nonspecific infection. The neurological deficit progresses in days and months. Material and Method: In this study, a total of 7 GBS cases with different clinical manifestations admitted to our clinic between 2016 and 2018 were presented. Results: Two patients were diagnosed with acute motor axonal neuropathy (AMAN), two patient with acute inflammatory demyelinating polyneuropathy (AIDP), one patient with Miller Fischer syndrome (MFS), one patient with Bickerstaff's brainstem encephalitis (BBE)and one patient with atypical Guillain Barre syndrome. The cases with AMAN necessitated respiratory support and ventilator-associated pneumonia and tension pneumothorax developed in one of them. Conclusion: All cases healed without any sequels.