Treatment of Kleine-Levin Syndrome with Acetazolamide

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Pharmacological 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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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...

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Differential 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.

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Kleine–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.

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A case of Kleine-Levin syndrome.

The positive correlation seen in the ER, PR scores and Her 2 neu amplification between the primary tumour and lymph node metastases and the absence of a significant difference between the score of ER, PR and the amplification of Her 2 neu between the primary tumour and the lymph node metastases indicates that there is a concordance in these parameters between the primary tumour and its nodal me...

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ژورنال

عنوان ژورنال: Journal of Clinical Sleep Medicine

سال: 2014

ISSN: 1550-9389,1550-9397

DOI: 10.5664/jcsm.4124