منابع مشابه
Guillain-Barré Syndrome (GBS) — Symptoms, Diagnosis and Variations
Inflammatory and immune-mediated polyneuropathies represent an important differential diagnosis of hereditary and acquired polyneuropathies. In this article, we will provide you with all the relevant facts concerning the GuillainBarré syndrome, the Miller-Fisher syndrome, and the Elsberg syndrome. Also, we will cover the chronic-inflammatory demyelinating polyneuropathy (CIDP) and multifocal mo...
متن کاملChronic Inflammatory Demyelinating Polyneuropathy in a Patient with Adenosine Deaminase Deficiency Severe Combined Immunodeficiency: Case Report
Adenosine deaminase deficiency is a type of severe combined immunodeficiency that involves about 15% of all SCID cases. This form of SCID has low B cells, T cells, and NK cells. This condition is complex with many possible complications including neurological abnormalities. Guillainbarré syndrome is an acute inflammatory disease of the peripheral nerves that involves an autoimmune attack on mye...
متن کاملGuillain-Barré Syndrome (GBS) — Symptoms, Diagnosis and Variations
Inflammatory and immune-mediated polyneuropathies represent an important differential diagnosis of hereditary and acquired polyneuropathies. In this article, we will provide you with all the relevant facts concerning the GuillainBarré syndrome, the Miller-Fisher syndrome, and the Elsberg syndrome. Also, we will cover the chronic-inflammatory demyelinating polyneuropathy (CIDP) and multifocal mo...
متن کاملGuillain-Barré Syndrome (GBS) — Symptoms, Diagnosis and Variations
Inflammatory and immune-mediated polyneuropathies represent an important differential diagnosis of hereditary and acquired polyneuropathies. In this article, we will provide you with all the relevant facts concerning the GuillainBarré syndrome, the Miller-Fisher syndrome, and the Elsberg syndrome. Also, we will cover the chronic-inflammatory demyelinating polyneuropathy (CIDP) and multifocal mo...
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ژورنال
عنوان ژورنال: BJA CEPD Reviews
سال: 2003
ISSN: 1472-2615
DOI: 10.1093/bjacepd/mkg012