0272 Sleep Loss May Mess With Premesntrual Syndromes In Dysmenorrheic Women
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چکیده
منابع مشابه
Diffuse hair loss in women in Ahwaz
Background: Diffuse hair loss is one of the most common complaints of women attending skin clinics. Objective: The purpose of this study was to evaluate diffuse hair loss in women referring to a private office. Patients and Methods: This descriptive, retrospective study was performed on women attending a private skin clinic in Ahwaz complaining of diffuse hair loss. The study was done for 10 mo...
متن کاملThe sleep apnoea syndromes.
In recent decades, awareness of sleep apnoea syndromes has increased both in the public mind and among medical professionals. As a result, the number of patients referred for evaluation to a sleep clinic has increased dramatically. The term sleep ‘disordered breathing’ comprises the whole continuum, from chronic snoring to obstructive sleep apnoea and the so-called ‘Pickwick syndrome’. Obstruct...
متن کاملObstructive sleep apnea syndromes.
The first description of an obstructive sleep apnea (OSA) sufferer is generally attributed to the novelist Charles Dickens, who described ‘‘Joe’’ in The Posthumous Papers of the Pickwick Club, published in 1836. Joe was an excessively sleepy, obese boy who snored loudly and had possible right-sided heart failure that led to his being called ‘‘young dropsy’’ [1,2]. The first physician to describ...
متن کاملSleep and epilepsy syndromes.
Sleep and epilepsy have a close relationship. About 20% of patients suffer seizures only during the night, approximately 40% only during the day and approximately 35% during the day and night. In certain epilepsy syndromes, the occurrence of seizures is strongly related to sleep or awakening. Infantile spasms appear predominately on awakening, and hypsarrhythmia is sometimes visible only in sle...
متن کاملTJP2 Gene Mutation c.G1012A May Responsible for Congenital Hearing Loss with Incomplete Penetrance in An Iranian Pedigree
Hereditary hearing loss (HHL) comprises half of the congenital deafness which arises from genetic mutations. Mutations in the TJP2 gene, encoding tight junction protein 2, are one of the gene alterations in HHL resulting in an autosomal dominant nonsyndromic form of the disease. An 11-year-old male patient with clinically approved congenital hearing loss was referred to our laboratory....
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ژورنال
عنوان ژورنال: Sleep
سال: 2019
ISSN: 0161-8105,1550-9109
DOI: 10.1093/sleep/zsz067.271