Gasser syndrome

ガッセル症候群。溶血性尿毒症症候群

WordNet

1. a pattern of symptoms indicative of some disease
2. a complex of concurrent things; "every word has a syndrome of meanings"

PrepTutorEJDIC

1. (疾患の徴候となる一群の)症徴候,症候群 / (事件・社会的状態などのパターンを示す)徴候形態

English Journal

• Modeling complement-driven diseases in transgenic mice: Values and limitations.

• Ueda Y1, Gullipalli D1, Song WC2.
• Immunobiology.Immunobiology.2016 Oct;221(10):1080-90. doi: 10.1016/j.imbio.2016.06.007. Epub 2016 Jun 16.
• Remarkable advances have been made over past decades in understanding the pathogenesis of complement-mediated diseases. This has led to development of new therapies for, and in some cases re-classification of, complement-driven diseases. This success is due to not only insight from human patients bu
• PMID 27371974

• Clinical Practice Guidelines for the Management of Atypical Hemolytic Uremic Syndrome in Korea.

• Cheong HI1,2, Jo SK3, Yoon SS4, Cho H5, Kim JS6, Kim YO7, Koo JR8, Park Y9, Park YS10, Shin JI11, Yoo KH12, Oh D13.
• Journal of Korean medical science.J Korean Med Sci.2016 Oct;31(10):1516-28. doi: 10.3346/jkms.2016.31.10.1516.
• Atypical hemolytic uremic syndrome (aHUS) is a rare syndrome characterized by micro-angiopathic hemolytic anemia, thrombocytopenia, and acute kidney injury. The major pathogenesis of aHUS involves dysregulation of the complement system. Eculizumab, which blocks complement C5 activation, has recently
• PMID 27550478

• Atypical hemolytic uremic syndrome: a clinical conundrum.

• Bajracharya P1, Jain A1, Baracco R1, Mattoo TK1, Kapur G2.
• Pediatric nephrology (Berlin, Germany).Pediatr Nephrol.2016 Oct;31(10):1615-24. doi: 10.1007/s00467-016-3369-6. Epub 2016 May 2.
• BACKGROUND: Patients negative for Shiga toxin-producing E. coli (STEC) are categorized as having atypical hemolytic uremic syndrome (HUS) and are associated with an increased risk for complement mutations and poorer prognosis compared with typical HUS. However, STEC identification is limited by the
• PMID 27139899

Japanese Journal

• Hamolytish-uremische syndrome: Bilaterale Nierenindennekrosen bei Akuten erworbenen Hamolytischen Anamien.

• Schweiz Med Wochenschr 85, 905-909, 1955
• NAID 10005563383

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★リンクテーブル★

リンク元	「溶血性尿毒症症候群」
関連記事	「syndrome」

「溶血性尿毒症症候群」

　　[★]

英

hemolytic uremic syndrome, HUS

同

ガッセル症候群 Gasser syndrome

関

血栓性血小板減少性紫斑病, thrombotic thrombocytopenic purpura, TTP

• 腸管出血性大腸菌 EHECの感染症患者のうち2-7%がHUSに移行する。特に15歳未満の小児、65歳以上の高齢者で発生率が高い。
• 溶血性貧血、血小板減少、急性腎不全
• 小児に多い。
• ベロ毒素→腎血管内皮細胞障害→内皮細胞の腫脹・剥離・内腔の狭小化、血栓形成

HUSの3徴候

let's memorize: The Fr.(=The franch)　←　TTPの5徴から精神症状と発熱を除いたもの

「syndrome」

　　[★]

• n.

• 症候群