{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,23]],"date-time":"2026-09-23T14:51:15Z","timestamp":1790175075046,"version":"4.1.0"},"reference-count":42,"publisher":"Wiley","issue":"7","license":[{"start":{"date-parts":[[2009,2,4]],"date-time":"2009-02-04T00:00:00Z","timestamp":1233705600000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["American J of Med Genetics Pt B"],"published-print":{"date-parts":[[2009,10,5]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>Autosomal recessive hereditary spastic paraplegia (ARHSP) with thin corpus callosum (TCC) is genetically heterogenous and approximately 35% of patients carry mutations in either of the <jats:italic>SPG11<\/jats:italic> or <jats:italic>SPG15<\/jats:italic> genes. Disease onset is during the first three decades of life with spastic paraplegia and mental impairment. Peripheral neuropathy and amyotrophy may occur. Kjellin syndrome is characterized by central retinal degeneration in addition to ARHSP\u2010TCC and the disease is associated with mutations in the <jats:italic>SPG15<\/jats:italic> gene. We identified five patients in four unrelated kindreds with spastic paraplegia and mental impairment. Magnetic resonance imaging revealed TCC, atrophy elsewhere in the brain and increased T2 signal intensity in the periventricular white matter. Probands from the four kindreds were screened for mutations in the <jats:italic>SPG11<\/jats:italic> gene. All patients were found homozygous or compound heterozygous for truncating <jats:italic>SPG11<\/jats:italic> mutations of which four are reported for the first time. Ophthalmological investigations revealed that the four index cases have central retinal degeneration consistent with Kjellin syndrome. PET examinations with <jats:italic>N<\/jats:italic>\u2010[11C\u2010methyl]\u2010<jats:sc>L<\/jats:sc>\u2010deuterodeprenyl (DED) and fluor\u201018 2\u2010fluorodeoxyglucose (FDG) were performed in two patients with Kjellin syndrome. We observed a reduced glucose uptake in the thalami, anterior cingulum, and sensorimotor cortex indicating neuronal loss, and an increased DED binding in the thalami and pons which suggests astrogliosis. From our results we extend the <jats:italic>SPG11<\/jats:italic> associated phenotype to comprise also Kjellin syndrome, previously found to be associated with mutations in the <jats:italic>SPG15<\/jats:italic> gene. We anticipate that degeneration of the central retina is a common and previously unrecognized feature in <jats:italic>SPG11<\/jats:italic> related disease. \u00a9 2009 Wiley\u2010Liss, Inc.<\/jats:p>","DOI":"10.1002\/ajmg.b.30928","type":"journal-article","created":{"date-parts":[[2009,2,4]],"date-time":"2009-02-04T15:00:53Z","timestamp":1233759653000},"page":"984-992","source":"Crossref","is-referenced-by-count":49,"title":["<i>SPG11<\/i> mutations cause Kjellin syndrome, a hereditary spastic paraplegia with thin corpus callosum and central retinal 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