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The phenotype of adult versus pediatric patients with inborn errors of metabolism
被引:13
|作者:
Saudubray, Jean-Marie
[1
]
Mochel, Fanny
[1
,2
,3
,4
,5
,6
,7
]
机构:
[1] Univ Paris 06, Grp Rech Clin Neurometab, Paris, France
[2] Grp Hosp Pitie Salpetriere, Ctr Reference Neurometab Adulte, Paris, France
[3] Sorbonne Univ, UPMC Paris 6, UMR S 1127, F-75013 Paris, France
[4] INSERM, U1127, F-75013 Paris, France
[5] CNRS, UMR 7225, F-75013 Paris, France
[6] ICM, F-75013 Paris, France
[7] Grp Hosp Pitie Salpetriere, AP HP, Dept Genet, Paris, France
关键词:
Inborn errors of metabolism;
Phenotypic variability;
Aging;
Genetic factors;
Ontogenic factors;
Environmental factors;
SOMATIC MOSAICISM;
LIVER-FAILURE;
DEFICIENCY;
MUTATIONS;
DISEASE;
HETEROZYGOSITY;
HYPERAMMONEMIA;
D O I:
10.1007/s10545-018-0209-9
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Until recently, inborn errors of metabolism (IEM) were considered a pediatric specialty, as emphasized by the term inborn, and the concept of adult onset IEM has only very recently reached the adult medical community. Still, an increasing number of adult onset IEM have now been recognized, as new metabolomics and molecular diagnostic techniques have become available. Here, we discuss possible mechanisms underlying phenotypic variability in adult versus children with IEM. Specifically, phenotypic severity and age of onset are expected to be modulated by differences in residual protein activity possibly driven by various genetic factors. Phenotypic variability may also occur in the context of similar protein expression, which suggests the intervention of environmental, ontogenic, and aging factors.
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页码:753 / 756
页数:4
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