Results 81 to 90 of about 164,986 (311)
ABSTRACT Schinzel‐Giedion Syndrome (SGS) is an ultra‐rare, multisystem, genetic developmental disorder caused by gain‐of‐function pathogenic variants in the SETBP1 gene. No standard of care (SoC) recommendations currently exist. To assess expert opinion on SoC for individuals with SGS using a modified Delphi method.
Jessica Duis+16 more
wiley +1 more source
Cardioversion of atrial fibrillation does not affect obstructive sleep apnea
Background: Sleep apnea is common in patients with atrial fibrillation, but the effect of the cardioversion of atrial fibrillation to sinus rhythm on central and obstructive apneas is mainly unknown.
Niklas Höglund+4 more
doaj +1 more source
ABSTRACT NM_000141.5: FGFR2 c.1032G>A is a pathogenic variant that causes Crouzon syndrome through activation of a new donor splice site. This clinical report highlights the intrafamilial variability that can exist with this specific variant. The proband is a 4‐year‐old boy who initially presented with concern for seizures.
Jessica T. Ogawa+3 more
wiley +1 more source
Background: Obstructive sleep apnea and stroke are the most common diseases worldwide and especially in our country. Previous studies showed that both above diseases are common risk factors and in some of study co-morbidity to stroke and obstructive ...
Mohammadreza Najafi, Sara Hoseinpour
doaj
Automatic scoring of apnea and hypopnea events using blood oxygen saturation signals [PDF]
The obstructive sleep apnea-hypopnea (OSAH) syndrome is a very common and frequently undiagnosed sleep disorder. It is characterized by repeated events of partial (hypopnea) or total (apnea) obstruction of the upper airway while sleeping. This study makes use of a previously developed method called DAS-KSVD for multiclass structured dictionary learning
arxiv
A Snoring Sound Dataset for Body Position Recognition: Collection, Annotation, and Analysis [PDF]
Obstructive Sleep Apnea-Hypopnea Syndrome (OSAHS) is a chronic breathing disorder caused by a blockage in the upper airways. Snoring is a prominent symptom of OSAHS, and previous studies have attempted to identify the obstruction site of the upper airways by snoring sounds.
arxiv
Children With 22.Q.11.2 Deletion Syndrome: Sleep‐Disordered Breathing and Management
ABSTRACT Patients with 22q11.2 deletion syndrome (22q11DS) are predisposed to obstructive sleep apnea (OSA) due to an abnormal craniofacial anatomy with pharyngeal hypotonia, retrognathia, micrognathia, and glossoptosis. The aim of the study was to describe the prevalence and management of OSA in a cohort of children with 22q11DS.
Domenico Paolo La Regina+6 more
wiley +1 more source
Introduction: Serum level of high-mobility group box 1 protein is reportedly correlated with the severity of obstructive sleep apnea. Objective: We tried to evaluate the possibility of using the serum high-mobility group box 1 protein level as a biologic
Hyun Jin Min+7 more
doaj
The aim. The study and analysis of cardiac arrhythmias, heart rhythm variability in patients with ischemic heart disease, obstructive sleep apnea and primary snoring. Material and methods.
E. S. Tarasik+2 more
doaj +1 more source
Rationale: Primary treatment of obstructive sleep apnea can be accompanied by a persistence of excessive sleepiness despite adherence. Furthermore, effectiveness of sleep apnea treatment is limited by poor adherence.
P. Schweitzer+10 more
semanticscholar +1 more source