Guillain Barré syndrome variant with facial diplegia and paresthesias: A case report and review of the literature
Journal Title: Ege Tıp Dergisi - Year 2015, Vol 54, Issue 2
Abstract
Guillain Barré syndrome (GBS) is a disorder characterized by areflexia and progressive ascending lower extremity weakness. Bilateral peripheral facial diplegia and paresthesia is a rare GBS variant in which the preceding infection, auto-antibody positivity and treatment models are still unclear. In this rare variant, no case with an etiology of varicella infection has been reported yet. Here, we report a case with facial diplegia and parestesia secondary to varicella infection and discuss clinical, electrophysiological and laboratory findings, and review the literature focusing on the latest reports on this disease.
Authors and Affiliations
Çetin Kürşad AKPINAR, Hakan DOĞRU, Ayşe Oytun BAYRAK, Hüseyin Alparslan ŞAHİN
Premature infant with neonatal abstinence syndrome
Neonatal abstinence syndrome (NYS) is a clinical condition characterized by physical dependence and withdrawal symptoms after prenatal exposure to addictive substances. These symptoms are self-limiting and usually do not...
Autologous stem cell transplantation as a consolidation therapy in acute myeloid leukemia patients
Aim: Autologous stem cell transplantation (ASCT) is a treatment option as a consolidation therapy in acute myeloid leukemia (AML) patients. ASCT may improve disease free survival without effecting overall survival rates...
Ekstübasyon aşamasında gelişen takotsubo sendromu: Olgu sunumu
Takotsubo sendromu sıklıkla yanlış tanı konulan, nadir bir hastalıktır. Sol ventrikülün apikal ve orta segmentlerinde geçici, reversibl bölgesel duvar hareket kusuru vardır ve elektrokardiyografi (EKG) değişiklikleri ile...
Primary carcinoid tumor of the testis: A rare case
Neuroendocrine tumors most commonly occur in the gastrointestinal tract, lungs and pancreas. Primary testicular neuroendocrine tumors are rare, constituting 0.23% of all testicular tumors. A 35-year-old man presented to...
Primary hyperoxaluria
Hyperoxaluria is characterized by nephrolithasis and nephrocalcinosis caused by supersaturation of calcium oxalate in the urine. Deposits of calcium oxalate can lead to kidney damage, kidney failure, and injury to other...