Copy number variation analysis using next-generation sequencing identifies the CFHR3/CFHR1 deletion in atypical hemolytic uremic syndrome: a case report

Objectives Atypical hemolytic uremic syndrome (aHUS) is characterized by a triad of thrombocytopenia, microangiopathic hemolytic anemia, and acute renal failure resulting from platelet thrombi in the microcirculation of the kidney and other organs, in the absence of a preceding diarrheal illness. Th...

ver descrição completa

Detalhes bibliográficos

Principais autores:	Joonhong Park, Ho-Young Yhim, Kyung Pyo Kang, Tae Won Bae, Yong Gon Cho
Formato:	Artigo
Idioma:	Inglês
Publicado em:	Taylor & Francis Group 2022-12-01
coleção:	Hematology
Assuntos:	Hemolytic uremic syndrome CFHR3/CFHR1 deletion next-generation sequencing copy number variation
Acesso em linha:	https://www.tandfonline.com/doi/10.1080/16078454.2022.2075121
Tags:	Adicionar Tag Sem tags, seja o primeiro a adicionar uma tag!