Idiopathic Hypersomnia
What's New
Last Posted: Jun 27, 2024
- High-resolution HLA sequencing and hypocretin receptor 2 autoantibodies in narcolepsy type 1 and type 2.
Samia Hamdan, et al. International journal of immunogenetics 2024 0 - Association between idiopathic hypersomnia and a genetic variant in the PER3 gene.
Yoan Cherasse, et al. Journal of sleep research 2024 0 e14146 - LMOD3 gene variant in familial periodic hypersomnolence.
Wenz Elena, et al. Sleep medicine 2022 0 105-108 - An association analysis of HLA-DQB1 with narcolepsy without cataplexy and idiopathic hypersomnia with/without long sleep time in a Japanese population.
Miyagawa Taku, et al. Human genome variation 2016 0 15031 - A missense variant in PER2 is associated with delayed sleep-wake phase disorder in a Japanese population.
Miyagawa Taku, et al. Journal of human genetics 2019 9 - Precision Medicine for Idiopathic Hypersomnia.
Arnulf Isabelle et al. Sleep medicine clinics 2019 Sep 14(3) 333-350 - Distribution of HLA-DQB1 in Czech Patients with Central Hypersomnias.
Vrana Milena, et al. Archivum immunologiae et therapiae experimentalis 2017 1 - Idiopathic hypersomnia
From NCATS Genetic and Rare Diseases Information Center - Narcolepsy with long sleep time: a specific entity?
Vernet Cyrille, et al. Sleep 2009 9 (9) 1229-35 - Prevalence of the HLA-DQB1*0602 allele in narcolepsy and idiopathic hypersomnia patients seen at a sleep disorders outpatient unit in São Paulo.
Coelho Fernando Morgadinho Santos, et al. Revista brasileira de psiquiatria (São Paulo, Brazil : 1999) 2009 3 (1) 10-4
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Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Eclampsia
- Erythema Multiforme
- Familial Mediterranean Fever
- Fragile X Syndrome
- Gaucher Disease
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- Graves Disease
- Hemophilia
- Huntington Disease
- Microcephaly
- Myasthenia Gravis
- Phenylketonuria
- Retinitis Pigmentosa
- Severe Combined Immunodeficiency
Disclaimer: Articles listed in the Public Health Knowledge Base are selected by Public Health Genomics Branch to provide current awareness of the literature and news. Inclusion in the update does not necessarily represent the views of the Centers for Disease Control and Prevention nor does it imply endorsement of the article's methods or findings. CDC and DHHS assume no responsibility for the factual accuracy of the items presented. The selection, omission, or content of items does not imply any endorsement or other position taken by CDC or DHHS. Opinion, findings and conclusions expressed by the original authors of items included in the update, or persons quoted therein, are strictly their own and are in no way meant to represent the opinion or views of CDC or DHHS. References to publications, news sources, and non-CDC Websites are provided solely for informational purposes and do not imply endorsement by CDC or DHHS.
- Page last reviewed:Feb 1, 2024
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