Further expanding the mutational spectrum of brain abnormalities, neurodegeneration, and dysosteosclerosis: A rare disorder with neurologic regression and skeletal features.
Erdem KindisPelin Özlem Şimsek KiperCan KoşukcuEkim Zihni TaşkiranRahşan GocmenGülen Eda UtineGöknur HaliloğluKoray BodurogluMehmet AlikaşifoğluPublished in: American journal of medical genetics. Part A (2021)
Colony stimulating factor 1 receptor (CSF1R, MIM# 164770) encodes a tyrosine-kinase receptor playing an important role in development of osteoclasts and microglia. Heterozygous CSF1R variants have been known to cause hereditary diffuse leukoencephalopathy with spheroids (HDLS, MIM# 221820), an adult-onset leukoencephalopathy characterized by loss of motor functions and cognitive decline. Recently, a new phenotype characterized by brain abnormalities, neurodegeneration, and dysosteosclerosis (BANDDOS) with biallelic CSF1R pathogenic variants in the etiology has been described. BANDDOS differs from HDLS by early-onset neurodegenerative changes with additional structural brain abnormalities and skeletal findings resembling dysosteosclerosis (DOS). Described skeletal findings of the disease are highly variable ranging from absence of a skeletal phenotype and milder Pyle disease-like to osteopetrosis and DOS. To date, only a few patients carrying biallelic CSF1R variants have been reported. In this clinical report, we describe three siblings with variable skeletal findings along with neurological symptoms ranging from mild to severe in whom exome sequencing revealed a novel homozygous splice site variant in canonical splice donor site of intron 21 adjacent to an exon, which encoding part of kinase domain of CSF1R along with a review of the literature.
Keyphrases
- early onset
- tyrosine kinase
- cognitive decline
- copy number
- resting state
- white matter
- late onset
- intellectual disability
- epidermal growth factor receptor
- end stage renal disease
- cerebral ischemia
- mild cognitive impairment
- functional connectivity
- single cell
- ejection fraction
- cerebrospinal fluid
- newly diagnosed
- chronic kidney disease
- inflammatory response
- gene expression
- neuropathic pain
- low grade
- multiple sclerosis
- protein kinase
- prognostic factors
- brain injury
- high grade