Please use this identifier to cite or link to this item: https://dora.health.qld.gov.au/qldresearchjspui/handle/1/7170
Title: Brain function in classic galactosemia, a galactosemia network (GalNet) members review
Authors: Panis, Bianca
Vos, E. Naomi
Barić, Ivo
Bosch, Annet M.
Brouwers, Martijn C. G. J.
Burlina, Alberto
Cassiman, David
Coman, David J.
Couce, María L.
Das, Anibh M.
Demirbas, Didem
Empain, Aurélie
Gautschi, Matthias
Grafakou, Olga
Grunewald, Stephanie
Kingma, Sandra D. K.
Knerr, Ina
Leão-Teles, Elisa
Möslinger, Dorothea
Murphy, Elaine
Õunap, Katrin
Pané, Adriana
Paci, Sabrina
Parini, Rossella
Rivera, Isabel A.
Scholl-Bürgi, Sabine
Schwartz, Ida V. D.
Sdogou, Triantafyllia
Shakerdi, Loai A.
Skouma, Anastasia
Stepien, Karolina M.
Treacy, Eileen P.
Waisbren, Susan
Berry, Gerard T.
Rubio-Gozalbo, M. Estela
Issue Date: 2024
Source: Frontiers in genetics, 2024 (15) p.1355962
Pages: 1355962
Journal Title: Frontiers in genetics
Abstract: Classic galactosemia (CG, OMIM #230400, ORPHA: 79,239) is a hereditary disorder of galactose metabolism that, despite treatment with galactose restriction, affects brain function in 85% of the patients. Problems with cognitive function, neuropsychological/social emotional difficulties, neurological symptoms, and abnormalities in neuroimaging and electrophysiological assessments are frequently reported in this group of patients, with an enormous individual variability. In this review, we describe the role of impaired galactose metabolism on brain dysfunction based on state of the art knowledge. Several proposed disease mechanisms are discussed, as well as the time of damage and potential treatment options. Furthermore, we combine data from longitudinal, cross-sectional and retrospective studies with the observations of specialist teams treating this disease to depict the brain disease course over time. Based on current data and insights, the majority of patients do not exhibit cognitive decline. A subset of patients, often with early onset cerebral and cerebellar volume loss, can nevertheless experience neurological worsening. While a large number of patients with CG suffer from anxiety and depression, the increased complaints about memory loss, anxiety and depression at an older age are likely multifactorial in origin.; Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. The author(s) declared that they were an editorial board member of Frontiers, at the time of submission. This had no impact on the peer review process and the final decision. (Copyright © 2024 Panis, Vos, Barić, Bosch, Brouwers, Burlina, Cassiman, Coman, Couce, Das, Demirbas, Empain, Gautschi, Grafakou, Grunewald, Kingma, Knerr, Leão-Teles, Möslinger, Murphy, Õunap, Pané, Paci, Parini, Rivera, Scholl-Bürgi, Schwartz, Sdogou, Shakerdi, Skouma, Stepien, Treacy, Waisbren, Berry and Rubio-Gozalbo.)
DOI: 10.3389/fgene.2024.1355962
Resources: https://search.ebscohost.com/login.aspx?direct=true&AuthType=ip,athens&db=mdc&AN=38425716&site=ehost-live
Appears in Sites:Children's Health Queensland Publications
Queensland Health Publications

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