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首页> 外文期刊>American Journal of Psychiatry and Neuroscience >A Biermer's Disease Revealed by a Myogeneous Syndrome About a Rare Case in Young African Black Subject and Literature Review
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A Biermer's Disease Revealed by a Myogeneous Syndrome About a Rare Case in Young African Black Subject and Literature Review

机译：由非洲年轻黑人受试者中罕见病例的肌综合征引起的比默氏病和文献综述

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摘要

Biermer's disease is an autoimmune disorder characterized by vitamin B12 deficiency. Neurological symptoms of B12 vitamin deficiency are polymorph. We report a case of a young black girl of 28 years old, senegalese student, consulted for walking ataxia and myalgia. The neurological examination found a myogenic syndrome of the four limbs. The electroneuromyogram showed diffuse myogenic involvement. The biological assessment found a macrocytic anemia at 112 fL with a vitamin B12 level collapsed at 74 pmol/L. The anti-parietal cell and anti-intrinsic factor were positive. Under supplementation with vitamin B12 the evolution is favorable after 8 months of treatment. Thus neurological deficiencies due to vitamin B12 deficiency are polymorphic. The dosage of vitamin B12 must be done before any neuropsychiatric symptoms that does not prove its worth.
机译：比尔默氏病是一种以维生素B12缺乏症为特征的自身免疫性疾病。 B12维生素缺乏症的神经症状是多形的。我们报告了一例塞内加尔学生，28岁的黑人少女，因行走共济失调和肌痛接受咨询。神经系统检查发现四肢肌源性综合征。肌电图显示弥漫性肌源性累及。生物学评估发现，巨细胞性贫血为112 fL，维生素B12水平降至74 pmol / L。抗壁细胞和抗内在因子均为阳性。在补充维生素B12的情况下，经过8个月的治疗，其发展良好。因此，由于维生素B12缺乏引起的神经系统缺陷是多态的。必须在任何不能证明其价值的神经精神症状之前服用维生素B12。

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