Chiari I Malformation in Nephropathic Cystinosis.
case_control · Level III
Where this comes from
- Record sourced from PubMed, PMID 26265281.
- Also identified by DOI 10.1016/j.jpeds.2015.07.038 and PMC identifier 4661060.
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Abstract
To determine the relative incidence of Chiari I malformations in children with cystinosis compared with those in the general population. Magnetic resonance imaging scans were performed on 53 patients with nephropathic cystinosis and 120 controls, age range 3-18 years. Ten of 53 (18.9%) patients with cystinosis had Chiari I or tonsillar ectopia, and only 2 of 120 controls (1.6%) had a similar finding. At least 2 of the patients had symptoms or signs thought to be related to the malformation, and one had surgical decompression. Two had an associated cervical syrinx. Children with cystinosis have a 12-fold higher prevalence of Chiari I malformations than the general pediatric population. Chiari I malformations should be high on the differential diagnosis when individuals with cystinosis develop neurologic signs and symptoms, and magnetic resonance imaging scans should be performed on children with cystinosis who present with new-onset headache, ataxia, incontinence, or other unexplained neurologic symptoms.
Medical subject headings
- Arnold-Chiari Malformation
- Cystinosis