Abstracts for the 45th Human Genetics Society of Australasia Annual Scientific Meeting, Perth, Western Australia, 24–27 November 2022.

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Zdroj: Twin Research & Human Genetics; Feb2023, Vol. 26 Issue 1, p49-126, 78p
Abstrakt: Young-Onset Dementia: A Systematic Review of the Psychosocial Impact on Genetic Relatives Maddison Wiggins SP 1,2 sp , Adrienne Sexton SP 1,3,4 sp and Alison McEwen SP 1 sp SP 1 sp Graduate School of Health, University of Technology Sydney, NSW, Australia, SP 2 sp St George Hospital, Sydney, NSW, Australia, SP 3 sp The Royal Melbourne Hospital, Melbourne, VIC, Australia, SP 4 sp The University of Melbourne, Melbourne, VIC, Australia I Background i : Young-onset dementia (YOD) describes a group of neurodegenerative conditions occurring before the age of 65, often caused by dominant genes such as I C9ORF72, PSEN1 i and I MAPT. i The social context of YOD creates extra psychological and social challenges, yet the experiences of at-risk relatives are often overlooked in society and healthcare settings. PLENARY 16 The Genetic Basis of Severe Childhood Speech Disorder Angela Morgan Murdoch Children's Research Institute, Melbourne, VIC, Australia, University of Melbourne, Melbourne, VIC, Australia, Royal Children's Hospital, Melbourne, VIC, Australia Childhood apraxia of speech (CAS), the prototypic severe childhood speech disorder, is characterized by motor programming and planning deficits. PLENARY 8 The Genetic Basis of Severe Childhood Speech Disorder Angela Morgan Murdoch Children's Research Institute, Melbourne, VIC, Australia, University of Melbourne, Melbourne, VIC, Australia, Royal Children's Hospital, Melbourne, VIC, Australia Childhood apraxia of speech (CAS), the prototypic severe childhood speech disorder, is characterized by motor programming and planning deficits. [Extracted from the article]
Databáze: Complementary Index