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Idiopathic hypersomnia
Author(s) -
BILLIARD MICHEL,
MERLE CORINNE,
CARLANDER BER TRAND,
ONDZE BASILE,
ALVAREZ DANIEL,
BESSET ALAIN
Publication year - 1998
Publication title -
psychiatry and clinical neurosciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.609
H-Index - 74
eISSN - 1440-1819
pISSN - 1323-1316
DOI - 10.1111/j.1440-1819.1998.tb00987.x
Subject(s) - narcolepsy , excessive daytime sleepiness , nap , pediatrics , medicine , psychology , polysomnography , sleep disorder , psychiatry , modafinil , insomnia , electroencephalography , neuroscience
Identification of idiopathic hypersomnia dates back 20 years only. It typically consists of prolonged nocturnal sleep, great difficulty waking up in the morning or at the end of a nap, and constant or recurrent excessive daytime sleepiness. Complete and incomplete forms are encountered. Twenty‐three subjects fulfilling ICSD criteria are reported with clinical, polysomnographic and immunogenetic data. Considering differential diagnosis is an important step in the diagnosis of idiopathic hypersomnia. Idiopathic hypersomnia is much less frequent than narcolepsy. A strong genetic component is suggested by the high proportion of familial cases. No association with HLA has been evidenced to date.

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