familial recurrent polyneuropathy

家族性再発性多発ニューロパチー

WordNet

1. relating to or having the characteristics of a family; "children of the same familial background"; "familial aggregation"
2. occurring among members of a family usually by heredity; "an inherited disease"; "familial traits"; "genetically transmitted features" (同)genetic, hereditary, inherited, transmitted, transmissible

PrepTutorEJDIC

1. 家族の,家族特有の / 違伝的な,血統にあらわれる
2. 再発する;繰り返し起こる

UpToDate Contents

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• 1. 多発性神経障害の概要 overview of polyneuropathy
• 2. 小児における後天性末梢性ニューロパチーの概要 overview of acquired peripheral neuropathies in children
• 3. シャルコーマリートゥース病などの一次性の遺伝性運動感覚性ニューロパチー hereditary primary motor sensory neuropathies including charcot marie tooth disease
• 4. 視神経症 optic neuropathies
• 5. 遺伝性ニューロパチーの概要 overview of hereditary neuropathies

English Journal

• Hypercoagulability in hereditary hemorrhagic telangiectasia with epilepsy.

• Finsterer J1, Sehnal E2.
• Journal of neurosciences in rural practice.J Neurosci Rural Pract.2015 Jul-Sep;6(3):407-9. doi: 10.4103/0976-3147.158791.
• Recent data indicate that in patients with hereditary hemorrhagic teleangiectasia (HHT), low iron levels due to inadequate replacement after hemorrhagic iron losses are associated with elevated factor-VIII plasma levels and consecutively increased risk of venous thrombo-embolism. Here, we report a p
• PMID 26167029

• PMP22-Related neuropathies and other clinical manifestations in Chinese han patients with charcot-marie-tooth disease type 1.

• Zhan Y1, Zi X1, Hu Z2, Peng Y2, Wu L2, Li X1, Jiang M1, Liu L1, Xie Y1, Xia K2, Tang B3, Zhang R1.
• Muscle & nerve.Muscle Nerve.2015 Jul;52(1):69-75. doi: 10.1002/mus.24550. Epub 2015 Mar 31.
• INTRODUCTION: Most cases of Charcot-Marie-Tooth (CMT) disease are caused by mutations in the peripheral myelin protein 22 gene (PMP22), including heterozygous duplications (CMT1A), deletions (HNPP), and point mutations (CMT1E).METHODS: Single-nucleotide polymorphism (SNP) arrays were used to study P
• PMID 25522693

• Adult-onset painful axonal polyneuropathy caused by a dominant NAGLU mutation.

• Tétreault M1, Gonzalez M2, Dicaire MJ1, Allard P3, Gehring K4, Leblanc D3, Leclerc N5, Schondorf R6, Mathieu J5, Zuchner S2, Brais B7.
• Brain : a journal of neurology.Brain.2015 Jun;138(Pt 6):1477-83. doi: 10.1093/brain/awv074. Epub 2015 Mar 28.
• Late-onset painful sensory neuropathies are usually acquired conditions associated with common diseases. Adult presentations of known hereditary forms are often accompanied by other organ involvement. We recruited a large French-Canadian family with a dominantly inherited late-onset painful sensory
• PMID 25818867

Japanese Journal

• Recurrent Cerebral Embolism in a Familial Amyloid Polyneuropathy Patient Who Received Partial Liver Transplantation from a Living Donor

• Internal medicine 40(3), 259-264, 2001-03
• NAID 10006999254

• かっ血，血たんを繰り返し経気管支肺生検にて肺病変を確認した家族性アミロイドポリニューロパシーの１例

• 日本内科学会雑誌 77(9), 1435-1439, 1988
• NAID 130000901149

Related Links

• Familial recurrent polyneuropathy. A family and a survey

Familial recurrent polyneuropathy. A family and a survey

• FAMILIAL RECURRENT POLYNEUROPATHY: A FAMILY ...

FAMILIAL RECURRENT POLYNEUROPATHY: A FAMILY AND A SURVEY 1 DORTHE ROOS, DORTHE ROOS Departments of Neurology, of the Rigshospitalet, Copenhagen, and the Gentofte Hospital Hellerup, Denmark 1 ...

• Familial amyloid polyneuropathy presenting as recurrent ...

Familial amyloid polyneuropathy presenting as recurrent hemoptysis and hemosputum: Detection of amyloid deposition of the lung by transbronchial lung biopsy Masashige MORITA 1) , Minoru HONGO 1) , Tomonobu KOIZUMI 1) , Eiichi GOMI 1) , Hiroshi KONO 1) , Yoshiki HIROSE 1) , Shinich OKUBO 1) , Shozo KUSAMA 1) , Ichiro MOCHIZUKI 2)

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リンク元	「家族性再発性多発ニューロパチー」
関連記事	「recurrent」「familial」

「家族性再発性多発ニューロパチー」

　　[★]

英

familial recurrent polyneuropathy

関

再発性多発ニューロパチー

「recurrent」

　　[★]

• adj.

• 反復性の、再発性の、反回性の、回帰の

関

iterative、recurrence、recurrently、regression、relapsing、repetitive

　

「familial」

　　[★]

• adj.

• 家族性の、家系性の、家族の

関

family、family member、household、kindred