The Genetics of Sleep Disorders in Children: A Narrative Review
Sleep is a universal, highly preserved process, essential for human and animal life, whose complete functions are yet to be unravelled. Familial recurrence is acknowledged for some sleep disorders, but definite data are lacking for many of them. Genetic studies on sleep disorders have progressed fro...
Ausführliche Beschreibung
Autor*in: |
Greta Mainieri [verfasserIn] Angelica Montini [verfasserIn] Antonio Nicotera [verfasserIn] Gabriella Di Rosa [verfasserIn] Federica Provini [verfasserIn] Giuseppe Loddo [verfasserIn] |
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E-Artikel |
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Sprache: |
Englisch |
Erschienen: |
2021 |
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Schlagwörter: |
sleep-related breathing disorders |
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Übergeordnetes Werk: |
In: Brain Sciences - MDPI AG, 2012, 11(2021), 10, p 1259 |
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Übergeordnetes Werk: |
volume:11 ; year:2021 ; number:10, p 1259 |
Links: |
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DOI / URN: |
10.3390/brainsci11101259 |
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Katalog-ID: |
DOAJ006019412 |
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10.3390/brainsci11101259 doi (DE-627)DOAJ006019412 (DE-599)DOAJd7a9ac9fa8bf44109e62ed6103ba860a DE-627 ger DE-627 rakwb eng RC321-571 Greta Mainieri verfasserin aut The Genetics of Sleep Disorders in Children: A Narrative Review 2021 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Sleep is a universal, highly preserved process, essential for human and animal life, whose complete functions are yet to be unravelled. Familial recurrence is acknowledged for some sleep disorders, but definite data are lacking for many of them. Genetic studies on sleep disorders have progressed from twin and family studies to candidate gene approaches to culminate in genome-wide association studies (GWAS). Several works disclosed that sleep-wake characteristics, in addition to electroencephalographic (EEG) sleep patterns, have a certain degree of heritability. Notwithstanding, it is rare for sleep disorders to be attributed to single gene defects because of the complexity of the brain network/pathways involved. Besides, the advancing insights in epigenetic gene-environment interactions add further complexity to understanding the genetic control of sleep and its disorders. This narrative review explores the current genetic knowledge in sleep disorders in children, following the International Classification of Sleep Disorders—Third Edition (ICSD-3) categorisation. insomnia sleep-related breathing disorders hypersomnolence circadian rhythm sleep-wake disorders parasomnias sleep-related movement disorders Neurosciences. Biological psychiatry. Neuropsychiatry Angelica Montini verfasserin aut Antonio Nicotera verfasserin aut Gabriella Di Rosa verfasserin aut Federica Provini verfasserin aut Giuseppe Loddo verfasserin aut In Brain Sciences MDPI AG, 2012 11(2021), 10, p 1259 (DE-627)687718139 (DE-600)2651993-8 20763425 nnns volume:11 year:2021 number:10, p 1259 https://doi.org/10.3390/brainsci11101259 kostenfrei https://doaj.org/article/d7a9ac9fa8bf44109e62ed6103ba860a kostenfrei https://www.mdpi.com/2076-3425/11/10/1259 kostenfrei https://doaj.org/toc/2076-3425 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 11 2021 10, p 1259 |
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10.3390/brainsci11101259 doi (DE-627)DOAJ006019412 (DE-599)DOAJd7a9ac9fa8bf44109e62ed6103ba860a DE-627 ger DE-627 rakwb eng RC321-571 Greta Mainieri verfasserin aut The Genetics of Sleep Disorders in Children: A Narrative Review 2021 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Sleep is a universal, highly preserved process, essential for human and animal life, whose complete functions are yet to be unravelled. Familial recurrence is acknowledged for some sleep disorders, but definite data are lacking for many of them. Genetic studies on sleep disorders have progressed from twin and family studies to candidate gene approaches to culminate in genome-wide association studies (GWAS). Several works disclosed that sleep-wake characteristics, in addition to electroencephalographic (EEG) sleep patterns, have a certain degree of heritability. Notwithstanding, it is rare for sleep disorders to be attributed to single gene defects because of the complexity of the brain network/pathways involved. Besides, the advancing insights in epigenetic gene-environment interactions add further complexity to understanding the genetic control of sleep and its disorders. This narrative review explores the current genetic knowledge in sleep disorders in children, following the International Classification of Sleep Disorders—Third Edition (ICSD-3) categorisation. insomnia sleep-related breathing disorders hypersomnolence circadian rhythm sleep-wake disorders parasomnias sleep-related movement disorders Neurosciences. Biological psychiatry. Neuropsychiatry Angelica Montini verfasserin aut Antonio Nicotera verfasserin aut Gabriella Di Rosa verfasserin aut Federica Provini verfasserin aut Giuseppe Loddo verfasserin aut In Brain Sciences MDPI AG, 2012 11(2021), 10, p 1259 (DE-627)687718139 (DE-600)2651993-8 20763425 nnns volume:11 year:2021 number:10, p 1259 https://doi.org/10.3390/brainsci11101259 kostenfrei https://doaj.org/article/d7a9ac9fa8bf44109e62ed6103ba860a kostenfrei https://www.mdpi.com/2076-3425/11/10/1259 kostenfrei https://doaj.org/toc/2076-3425 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 11 2021 10, p 1259 |
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Sleep is a universal, highly preserved process, essential for human and animal life, whose complete functions are yet to be unravelled. Familial recurrence is acknowledged for some sleep disorders, but definite data are lacking for many of them. Genetic studies on sleep disorders have progressed from twin and family studies to candidate gene approaches to culminate in genome-wide association studies (GWAS). Several works disclosed that sleep-wake characteristics, in addition to electroencephalographic (EEG) sleep patterns, have a certain degree of heritability. Notwithstanding, it is rare for sleep disorders to be attributed to single gene defects because of the complexity of the brain network/pathways involved. Besides, the advancing insights in epigenetic gene-environment interactions add further complexity to understanding the genetic control of sleep and its disorders. This narrative review explores the current genetic knowledge in sleep disorders in children, following the International Classification of Sleep Disorders—Third Edition (ICSD-3) categorisation. |
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Sleep is a universal, highly preserved process, essential for human and animal life, whose complete functions are yet to be unravelled. Familial recurrence is acknowledged for some sleep disorders, but definite data are lacking for many of them. Genetic studies on sleep disorders have progressed from twin and family studies to candidate gene approaches to culminate in genome-wide association studies (GWAS). Several works disclosed that sleep-wake characteristics, in addition to electroencephalographic (EEG) sleep patterns, have a certain degree of heritability. Notwithstanding, it is rare for sleep disorders to be attributed to single gene defects because of the complexity of the brain network/pathways involved. Besides, the advancing insights in epigenetic gene-environment interactions add further complexity to understanding the genetic control of sleep and its disorders. This narrative review explores the current genetic knowledge in sleep disorders in children, following the International Classification of Sleep Disorders—Third Edition (ICSD-3) categorisation. |
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Sleep is a universal, highly preserved process, essential for human and animal life, whose complete functions are yet to be unravelled. Familial recurrence is acknowledged for some sleep disorders, but definite data are lacking for many of them. Genetic studies on sleep disorders have progressed from twin and family studies to candidate gene approaches to culminate in genome-wide association studies (GWAS). Several works disclosed that sleep-wake characteristics, in addition to electroencephalographic (EEG) sleep patterns, have a certain degree of heritability. Notwithstanding, it is rare for sleep disorders to be attributed to single gene defects because of the complexity of the brain network/pathways involved. Besides, the advancing insights in epigenetic gene-environment interactions add further complexity to understanding the genetic control of sleep and its disorders. This narrative review explores the current genetic knowledge in sleep disorders in children, following the International Classification of Sleep Disorders—Third Edition (ICSD-3) categorisation. |
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