CSF1R-related brain malformation and osteopetrosis

Summary
Synonym
  • osteoporosis and infantile neuroaxonal dystrophy
Definition
A neuroaxonal dystrophy that has_material_basis_in heterozygous mutations in CSF1R and causes adult-onset leukoencephalopathy with axonal spheroids and pigmented glia, characterized by progressive cognitive and motor impairment and seizures in the fourth to fifth decade of life.
Super Class
neuroaxonal dystrophy
Disease Ontology
DOID:0070343

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: April 7, 2025