A case of acquired lecithin:cholesterol acyltransferase deficiency with sarcoidosis that remitted spontaneously

Familial lecithin:cholesterol acyltransferase (LCAT) deficiency is a rare inherited disorder that causes an extremely low high-density lipoprotein cholesterol concentration in serum. Recently, acquired LCAT deficiency caused by IgG antibodies to LCAT, without any LCAT gene mutation, was reported. He...

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Detalhes bibliográficos
Publicado no:CEN Case Rep
Main Authors: Akiko, Tanino, Okura, Takafumi, Nagao, Tomoaki, Kukida, Masayoshi, Enomoto, Daijiro, Miyoshi, Ken-ichi, Higaki, Jitsuo, Kuroda, Masayuki, Bujo, Hideaki
Formato: Artigo
Idioma:Inglês
Publicado em: Springer Japan 2016
Assuntos:
Case Report
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5411646/
https://ncbi.nlm.nih.gov/pubmed/28508975
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s13730-016-0223-4
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