Original Articles
Inborn errors of metabolism in the Italian pediatric population: A national retrospective survey

https://doi.org/10.1067/mpd.2002.122394Get rights and content

Abstract

Objective: To estimate at the national level the overall and diseasespecific incidence of inborn errors of metabolism not mass screened at birth. Study design: Prospective nonconcurrent study (1985-1997) on patients 0 to 17 years of age, diagnosed in 23 Italian pediatric reference centers. Results: Cases (n = 1935) were recruited representing an incidence of 1:3707 live births for ∼200 diseases. In the last 5 years the incidence was 1:2758, reflecting improved diagnostic facilities, better coverage, increased medical awareness, and newly discovered diseases. In this period, the most frequent classes of diseases were lysosomal storage disease, 1:8275; disorders of carbohydrate metabolism, 1:19,532; organic acidopathies, 1:21,422; and primary lactic acidemias, 1:27,106. The most frequent individual diseases were Gaucher type I, 1:40,247; glycogenosis type 1a, 1:57,746; methylmalonic acidurias, 1:61,775; and ornithine transcarbamylase deficiency, 1:69,904. The incidence of diseases potentially identifiable with the use of a new neonatal mass screening technique is 1:6200. Of surviving patients, 11% reached adulthood by the end of the study. Conclusions: Inborn errors of metabolism constitute a highly heterogeneous category of rare diseases, representing a relevant cause of morbidity and mortality in childhood. This study quantifies the minimum size of the disease burden, providing useful tools for public health and health policy planning. (J Pediatr 2002;140:321-7)

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Cited by (191)

  • Extended Risk of Mortality in Children with Inborn Errors of Metabolism: A Longitudinal Cohort Study

    2023, Journal of Pediatrics
    Citation Excerpt :

    In our data, children with isolated inborn errors had greater mortality than children affected solely by preterm birth or birth defects. Previous studies have not considered the effect of preterm birth or birth defects,4-10 even though these conditions are risk factors for chronic morbidity and mortality,14,15 and are common in children with inborn errors.21,24-26 Nevertheless, our results suggest that preterm birth and congenital anomalies do not make a major contribution to mortality beyond the effect of inborn errors of metabolism.

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Supported by the Italian Ministry of Health, grant ICS 120.2/RF96.349.

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