Inflammatory myopathy in a patient with Aicardi-Goutières syndrome

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منابع مشابه

[Aicardi-Goutières syndrome].

INTRODUCTION Aicardi-Goutières syndrome (AGS) is an autosomal recessive encephalopathy characterized by acquired microcephaly, cerebral calcifications, leukodystrophy, cerebral atrophy and cerebrospinal fluid findings of chronic lymphocytosis and raised interferon-alpha (INF-alpha). The main extraneurological symptoms are chilblain-like skin lesions, usually on the fingers, toes and ears. SOU...

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Aicardi-Goutières syndrome.

Aicardi-Goutieres syndrome is a familial progressive early onset encephalopathy with basal ganglia calcifications, chronic CSF lymphocytosis and high level of interferon-alpha in CSF. Cutaneous necrotic lesions and the neuropathological aspect of microangiopathy and microinfarctions suggest a vascular process in relation to elevated interferon-alpha. A genetic defect in the regulation of its sy...

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Interferon and Aicardi-Goutières syndrome.

There are two types of interferon (IFN), as you know already, and the interferon which we are interested in for this syndrome is type 1 IFN, specifically the alpha type. Interferons are proteins produced by the host in response to viral infection. Interferon alpha and beta(type I) are not normally detected in blood of healthy people, but they are found mostly in different specimens of patients ...

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Adult-onset dystonia in Aicardi-Goutières syndrome.

Aicardi-Goutières syndrome (AGS) is a rare, genetically determined encephalopathy with features mimicking congenital infection (microcephaly, bilateral basal ganglia calcifications, cerebral white matter abnormalities, cerebral atrophy, chronic CSF lymphocytosis, and elevated CSF INF-a). Disease onset usually occurs during the first year of life as a subacute encephalopathy and then the clinica...

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Gastric Strongyloides Stercoralis in a Patient with Inflammatory Myopathy

Strongyloides stercoralis is a free living tropical and semitropical soil nematode which its larva penetrates skin. It can complete its life cycle in human body and causes autoinfection. Most patients have no frank symptoms. But respiratory, gastrointestinal and skin manifestation may occur. We report a 76 year old man admitted to emergency room with muscle weakness, dyspnea, nausea, v...

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ژورنال

عنوان ژورنال: European Journal of Medical Genetics

سال: 2017

ISSN: 1769-7212

DOI: 10.1016/j.ejmg.2016.12.004