Results 41 to 50 of about 6,218 (123)

Relationship between enuresis and obstructive sleep apnea–hypopnea syndrome in children

Journal of International Medical Research, 2020
Objective We explored the relationship between enuresis and obstructive sleep apnea–hypopnea syndrome (OSAHS) in children and influencing factors of enuresis with OSAHS.
Chen Sun, Yingpeng Xu, Chenxi Luo, Qi Li
doaj   +1 more source

Management of Monosymptomatic Nocturnal Enuresis in Children: A Pilot Randomised Control Trial of Body‐Worn Versus Bell‐and‐Pad Alarm Device

Journal of Paediatrics and Child Health, EarlyView.
ABSTRACT Aim To compare bell‐and‐pad alarm therapy to body‐worn alarm therapy for the management of monosymptomatic enuresis in children 6–16 years of age in Victoria, Australia. Method A sample of 76 children with monosymptomatic enuresis were randomly allocated to a control group (bell‐and‐pad alarm, n = 38) or an experimental group (body‐worn alarm,
Blake Peck, Daniel Terry, Bronwyn Peck, Andrea Green, Kerrie Svedas, Shirley Whitaker, Monica Harrop, Erica Pearce, Mark Nethercote, Natasha Burgess, Ha N. D. Le, Sithara Wanni Arachchige Dona, Susan Gibb   +12 more
wiley   +1 more source

Resolution of enuresis after adenotsillectomy in children with adenotonsillar hypertrophy [PDF]

Iranian Journal of Otorhinolaryngology, 2008
Introduction: Most of the upper airway obstructions are caused by adenotonsillar hypertrophy. Prevalence of nocturnal enuresis in children accompanied with upper airway obstruction is reported in 8-47% of cases.
Mohammad Naeimi, Mohammad ali Mohammadzadeh Rezaei, adeleh Hajizadeh   +2 more
doaj  

Prevalence of Nocturnal Enuresis and Its Associated Factors in Primary School and Preschool Children of Khorramabad in 2013

International Journal of Pediatrics, 2014
Background. Nocturnal enuresis refers to an inability to control urination during sleep. This study aimed to determine the prevalence of nocturnal enuresis and its associated factors in children in the city of Khorramabad. Materials and Methods.
Katayoun Bakhtiar, Yadollah Pournia, Farzad Ebrahimzadeh, Ali Farhadi, Fathollah Shafizadeh, Reza Hosseinabadi   +5 more
doaj   +1 more source

Parasomnias and sleep‐related movement disorders induced by drugs in the adult population: a review about iatrogenic medication effects

Journal of Sleep Research, Volume 34, Issue 2, April 2025.
Summary Parasomnias and sleep‐related movement disorders (SRMD) are major causes of sleep disorders and may be drug induced. The objective of this study was to conduct a systematic review of the literature to examine the association between drug use and the occurrence of parasomnias and SRMD.
Sylvain Dumont, Vanessa Bloch, Agnès Lillo‐Lelouet, Christine Le Beller, Pierre A. Geoffroy, Marc Veyrier   +5 more
wiley   +1 more source

Impact of Hypoxemia Severity on Cardiac Autonomic Regulation in Children With Sleep‐Disordered Breathing: A McGill Oximetry‐Based Analysis

Journal of Sleep Research, EarlyView.
ABSTRACT Sleep‐related breathing disorders (SRBD) represent a significant paediatric health concern. Traditional polysomnographic indices, such as the apnoea–hypopnoea index, may not fully capture the physiological burden of paediatric SRBD, highlighting the need to better characterise the impact of nocturnal hypoxemia on cardiac autonomic regulation ...
Gintare Oboleviciene, Ausra Snipaitiene, Valdone Miseviciene   +2 more
wiley   +1 more source

ENURESIS AND ITS COMPLICATIONS

, 2023
<p>This article summarizes the study of the examination of the patient, work with medical records, observation, analysis of scientific literature. We examined 100 children with enuresis aged 5 to 15 years.
Jalilov Asliddin Xolmatovich, Islamov Nurali Hikmatovich, Najimov Shoxboz Raximjon o'g'li   +2 more
core   +1 more source

Distinct Neuropsychiatric Profiles Associated With 17p11.2 Deletions and RAI1 Variants in Smith–Magenis Syndrome

American Journal of Medical Genetics Part A, Volume 200, Issue 10, Page 2320-2330, October 2026.
ABSTRACT Smith–Magenis syndrome (SMS) results from either a recurrent 17p11.2 deletion or pathogenic variants in the retinoic acid induced 1 gene (RAI1). While neurodevelopmental impairment and behavioral dysregulation are well recognized, systematic genotype‐stratified analyses across psychiatric domains remain limited.
Albin Blanc, Christophe Nemos, Céline Bonnet, Mathilde Renaud, Sandra Chapuis, Pauline Boiroux, Marie‐Noëlle Babinet, Caroline Demily   +7 more
wiley   +1 more source

Sleep in Young Children With Autism, ADHD and Combined Presentations

Autism Research, Volume 19, Issue 9, September 2026.
ABSTRACT Autism and attention deficit hyperactivity disorder (ADHD) are often accompanied by sleep problems. Longitudinal studies hint towards a greater proportion of persisting sleep problems across early development in neurodivergent compared to neurotypical individuals. Within the context of a prospective infant sibling study of autism and ADHD (n = 
Eva‐Maria Kurz, Sven Bölte, Terje Falck‐Ytter   +2 more
wiley   +1 more source

Optical mapping reveals a higher level of large‐scale structural variants in a family with paternally transmitted myotonic dystrophy and independent Parkinson's disease

The Journal of Pathology, Volume 270, Issue 1, Page 83-97, September 2026.
Abstract Myotonic dystrophy type 1 (DM1) is a clinically challenging multisystem neuromuscular hereditary disorder, with generational increase in severity and earlier age at onset. It is caused by an unstable cytosine‐thymine‐guanine repeat expansion at the DMPK locus, accompanied by associated genetic and epigenetic modifications.
Md Mehedi Hasan, Jenna Craddock, Tingting Gong, Ruth J Lyons, Igor Stevanovski, Sanjog R Chintalaphani, Ira W Deveson, Weerachai Jaratlerdsiri, Kishore R Kumar, Vanessa M Hayes   +9 more
wiley   +1 more source