https://ogma.newcastle.edu.au/vital/access/ /manager/Index ${session.getAttribute("locale")} 5 Molecular and clinical characterization of a series of patients with childhood-onset lysosomal acid lipase deficiency. Retrospective investigations, follow-up and detection of two novel LIPA pathogenic variants https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:31058 A variant was observed in homozygosity or compound heterozygosity in 10 patients. We found seven previously reported variants: p.(Trp140*), p.(Arg218*), p.(Gly266*), p.(Thr288Ile), p.(Leu294Ser), p.(His295Tyr) and p.(Gly342Arg) and two novel variants: p.(Asp345Asn), affecting the LAL catalytic triad, and c.229+3A > C, affecting splicing. Homozygosity for p.(Thr288Ile) or c.229+3A > C was associated with a severe phenotype. Conclusions: This study provides additional data on the features of childhood-onset LAL-D and describes two novel pathogenic variants of the LIPA gene.]]> Thu 03 Feb 2022 12:18:33 AEDT ]]> Associations Between Hyperphagia, Symptoms of Sleep Breathing Disorder, Behaviour Difficulties and Caregiver Well-Being in Prader-Willi Syndrome: A Preliminary Study https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:44807 Mon 24 Oct 2022 09:31:54 AEDT ]]> Daytime sleepiness and emotional and behavioral disturbances in Prader-Willi syndrome https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:52313 Mon 09 Oct 2023 10:23:33 AEDT ]]> Requirements for improving health and well-being of children with Prader-Willi syndrome and their families https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:45712 Fri 04 Nov 2022 10:23:59 AEDT ]]>