منابع مشابه
Kleine-Levin syndrome: a review
Kleine-Levin syndrome is a recurrent hypersomnia associated with symptoms of hyperphagia, hypersexuality, and cognitive impairment. This article reviews the current available research and describes common clinical symptoms, differential diagnosis, and acceptable workup and treatment. Although deficits have traditionally been thought to resolve between episodes, functional imaging studies and lo...
متن کاملDifferential Diagnosis of Kleine-Levin Syndrome
Investigators at Pitie-Salpetriere and Robert Debre Hospitals, and other centers in France, evaluated consecutive patients referred for suspected Kleine-Levin (KLS) syndrome, detailed differential diagnoses, and examined characteristics of patients with prolonged (>30 days) episodes.
متن کاملKleine–Levin Syndrome: A case report☆
Kleine-Levin Syndrome is an unusual sleep disorder occurring predominantly, but not exclusively, in late adolescent males. A case is described which illustrates some of the difficulties in diagnosis and management.
متن کاملMonozygotic twins concordant for Kleine-Levin syndrome
BACKGROUND Kleine-Levin syndrome is a rare sleep disorder of unknown etiology. It is characterized by intermittent periods of excessive sleepiness, cognitive disturbances and behavioral abnormalities. Nine cases of familial Kleine-Levin syndrome have been identified, but there are no reported cases describing twins that are affected by the syndrome. CASE PRESENTATION We report the cases of 16...
متن کاملPharmacological treatment for Kleine-Levin syndrome.
BACKGROUND This is an updated version of the original Cochrane review, published in 2009, Issue 2.Kleine-Levin syndrome (KLS) is a rare disorder that mainly affects adolescent men. It is characterised by recurrent episodes of hypersomnia, usually accompanied by hyperphagia, cognitive and mood disturbances, abnormal behaviour, such as hypersexuality, and signs of dysautonomia.In 1990, the diagno...
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ژورنال
عنوان ژورنال: DMW - Deutsche Medizinische Wochenschrift
سال: 1914
ISSN: 0012-0472,1439-4413
DOI: 10.1055/s-0029-1190683