Atypical Hemolytic–Uremic Syndrome  

Oleh:

Noris, Marina ; Remuzzi, Giuseppe

Jenis: Article from Journal - ilmiah internasional
Dalam koleksi: The New England Journal of Medicine (keterangan: ada di Proquest) vol. 361 no. 17 (Oct. 2009), page 1676-168.
Topik: Uremic

Ketersediaan

Perpustakaan FK Nomor Panggil: N08.K.2009.05 Non-tandon: 1 (dapat dipinjam: 0) Tandon: tidak ada

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Isi artikel

The hemolytic–uremic syndrome is characterized by nonimmune hemolytic anemia, thrombocytopenia, and renal impairment. The disorder occurs most frequently in children under the age of 5 years, with an annual incidence of 6.1 cases per 100,000 children under 5 years, as compared with an overall incidence of 1 to 2 cases per 100,000. The presentation is generally heralded by diarrhea, which is often bloody. Most cases (including more than 90% of those in children) are secondary to infection with Escherichia coli serotypes O157:H7, O111:H8, O103:H2, O123, O26, or others, which produce Shiga-like toxin (Stx), and several other bacteria, such as Streptococcus pneumoniae.

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