Mevalonic aciduria and hyper-IgD syndrome: Two sides of the same coin?

被引：13

作者：

Tsimaratos, M ^{[1
]}

Kone-Paut, I

Divry, P

Philip, N

Chabrol, B

机构：

[1] Grp Hosp Timone, Hop Enfants, Serv Pediat Multidisciplinaire, Unite Nephrol, F-13385 Marseille 05, France

[2] Hop Nord Marseille, Serv Pediat, Marseille, France

[3] Hop Debrousse, Serv Biochim, Lyon, France

[4] Grp Hosp Timone, Hop Enfants, Serv Genet, Marseille, France

[5] Grp Hosp Timone, Hop Enfants, Serv Neurol Pediat, Marseille, France

来源：

JOURNAL OF INHERITED METABOLIC DISEASE | 2001年 / 24卷 / 03期

关键词：

D O I：

10.1023/A:1010577207726

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

[No abstract available]

引用

页码：413 / +

页数：2

共 6 条

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HOFFMANN GF, 1993, PEDIATRICS, V91, P915

[4] Mutations in MVK, encoding mevalonate kinase, cause hyperimmunoglobulinaemia D and periodic fever syndrome [J].

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[5] MEVALONIC ACIDURIA IN 3 SIBLINGS - A NEW RECOGNIZABLE METABOLIC ENCEPHALOPATHY [J].

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[6] Crescentic glomerulonephritis in hyper IgD syndrome [J].

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PEDIATRIC NEPHROLOGY, 1999, 13 (02) :132-134

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