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. 2010 Aug 24;75(8):718-25.
doi: 10.1212/WNL.0b013e3181eee46b. Epub 2010 Jul 21.

The burden of inherited leukodystrophies in children

Affiliations

The burden of inherited leukodystrophies in children

J L Bonkowsky et al. Neurology. .

Abstract

Objectives: Leukodystrophies are diseases of the white matter for which data concerning clinical characteristics, incidence, disease burden, and description of outcomes are sparse. The purpose of our study was to determine the incidence and most common types of inherited leukodystrophies in a population, the mortality and time course of deaths, common neurologic features in patients, and health care costs associated with leukodystrophies.

Methods: We conducted a retrospective, hospital- and clinic-based surveillance of inherited leukodystrophies among children younger than 18 years presenting to a regional children's hospital. We enrolled children evaluated from January 1, 1999, through December 31, 2007; clinical information was obtained from medical records. We calculated incidence based on state birth rates.

Results: A total of 122 children with an inherited leukodystrophy were identified; 542 patients were excluded. A total of 49% had epilepsy, 43% required a gastrostomy tube, and 32% had a history of developmental regression. Mortality was 34%; average age at death was 8.2 years. No final diagnosis was reported in 51% of patients. The most common diagnoses were metachromatic leukodystrophy (8.2%), Pelizaeus-Merzbacher disease (7.4%), mitochondrial diseases (4.9%), and adrenoleukodystrophy (4.1%). Endocrine abnormalities and hypoplastic cerebellum were noted in significant portions of patients (15% and 14%). Average yearly per-patient medical costs were $22,579. Population incidence was 1 in 7,663 live births.

Conclusions: Inherited leukodystrophies are associated with substantial morbidity and mortality in children. Overall population incidence is higher than generally appreciated (1 in 7,663 live births). Most leukodystrophies remain undiagnosed, but a logical algorithm based on prevalence could aid testing.

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Figures

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Figure 1 Leukodystrophy cohort epilepsy, deaths, and costs Number of new epilepsy cases (A) and deaths (B) shown by age. Vertical axis: number of cases. Underlying diagnosis is color-coded, key to right of graphs. (C) Total costs per patient, in thousands of dollars. Cumulative percentage of patients represented is indicated by solid line. ALD = adrenoleukodystrophy; MLD = mitochondrial disease; PMD = Pelizaeus-Merzbacher disease.

References

    1. Berger J, Moser HW, Forss-Petter S. Leukodystrophies: recent developments in genetics, molecular biology, pathogenesis and treatment. Curr Opin Neurol 2001;14:305–312. - PubMed
    1. Kaye EM. Update on genetic disorders affecting white matter. Pediatr Neurol 2001;24:11–24. - PubMed
    1. Miller DH, Robb SA, Ormerod IE, et al. Magnetic resonance imaging of inflammatory and demyelinating white-matter diseases of childhood. Dev Med Child Neurol 1990;32:97–107. - PubMed
    1. Schiffmann R, van der Knaap MS. An MRI-based approach to the diagnosis of white matter disorders. Neurology 2009;72:750–759. - PMC - PubMed
    1. van der Knaap MS, Breiter SN, Hart AAM, Valk J. Defining and categorizing leukoencephalopathies of unknown origin: MR imaging approach. Radiology 1999;213:121–133. - PubMed

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