Verny Christophe, Prundean Adriana, Nicolas Guillaume, Pautot Vivien, Maugin Dominique, Levade Thierry, Bonneau Dominique, Dubas Frederic
Centre national de référence des maladies neurogénétiques et cytopathies mitochondriales de l'adulte, Centre Hospitalier Universitaire, Angers, France.
Neuromuscul Disord. 2006 Nov;16(11):805-8. doi: 10.1016/j.nmd.2006.07.001. Epub 2006 Aug 23.
Refsum's disease is a rare autosomal recessive disorder with clinical features including retinitis pigmentosa, anosmia, deafness, chronic sensory-motor neuropathy, ataxia and the accumulation of phytanic acid in blood plasma and body tissues. We report the occurrence of Refsum's disease in two sisters, both presenting with acute demyelinating polyneuropathy mimicking the familial Guillain Barre syndrome. Thus, when GBS is suspected, particularly in cases of familial recurrence as well as in atypical cases of acute polyneuropathy, the diagnosis of Refsum's disease should be considered, looking for other features of the disease and, if appropriate, testing plasma phytanic acid levels.
雷夫叙姆病是一种罕见的常染色体隐性疾病,其临床特征包括色素性视网膜炎、嗅觉丧失、耳聋、慢性感觉运动性神经病变、共济失调以及血浆和身体组织中植烷酸的蓄积。我们报告了两姐妹患雷夫叙姆病的病例,她们均表现为急性脱髓鞘性多发性神经病变,类似于家族性格林-巴利综合征。因此,当怀疑格林-巴利综合征时,尤其是在家族复发病例以及急性多发性神经病变的非典型病例中,应考虑雷夫叙姆病的诊断,寻找该疾病的其他特征,并在适当情况下检测血浆植烷酸水平。