Results 41 to 50 of about 67,462 (202)

NOCTURNAL ENURESIS AND ITS RELATION TO CHILD’S BEHAVIOR IN A SAMPLE OF CHILDREN FROM BAGHDAD, IRAQ

The Iraqi Journal of Medical Sciences, 2016
Background:Nocturnal enuresis is one of common clinical problems in pediatric population that frequently diagnosed among school age children. Objectives:To determine the prevalence of nocturnal enuresis, to detect the socio-demographic factors that may ...
Alaa A. Saleh, Atheer J. Al-Saffar
doaj   +4 more sources

Evaluation of the Frequency of Obesity and Demographic Characteristics of Children with Primary Monosymptomatic Nocturnal Enuresis

Haseki Tıp Bülteni, 2017
Methods: Seventy healthy children and 70 nocturnal enuresis patients were compared in terms of age, gender, body weight, height, body mass index (BMI), BMI standard deviation score, obesity, maternal age and education level, father’s age and education ...
Gamze Sarıkaya Uzan, Bağdagül Yavaş Aksu, Muhammed Mustafa Uzan, Murat Elevli   +3 more
doaj   +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

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

Epidemiology of Enuresis among Children in Diyala Governorate

Diyala Journal of Medicine, 2021
Background: Nocturnal enuresis, is intermittent involuntary voiding in a child aged five years or more. One time a month for three months is required for the diagnosis. It is a common problem in children. It is the cause of stress for them and for their
Enas S Salahaldeen , Nadhim Gh Noaman , Mehdi SH Al-Zuheiry   +2 more
doaj   +2 more sources

The epidemiology and factors associated with nocturnal enuresis among boarding and daytime school children in southeast of Turkey: a cross sectional study

BMC Public Health, 2009
Background Nocturnal enuresis is an important problem among young children living in Turkey. The purpose of this study was to determine the possible differences in the prevalence of enuresis between children in boarding school and daytime school and the ...
Acik Yasemin, Gunes Gulsen, Gunes Ali, Akilli Adem   +3 more
doaj   +1 more source

Impact of an Educational Program on Mothers' Knowledge, Attitude and Practice Regarding Their Children with Nocturnal Enuresis [PDF]

Egyptian Journal of Health Care, 2016
Introduction:- Child enuresis is a widespread problem that can be upsetting for children andtheir families. Design:- The present study is a quasi-experimental one, aimed to provide aneducational program for mothers to enhance their knowledge, attitude ...
Neama Mohamed Fouad Kamel, Safaa Abdelazem Osman Ali, Zeinab Hassan Hassan Osman   +2 more
doaj   +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

Utility of Voiding Dysfunction Symptom Score in Diagnosis and Treatment of Enuresis Nocturna

Journal of Urological Surgery, 2017
Objective: The aim of this study was to determine the effectiveness of the voiding dysfunction symptom score (VDSS) in evaluation of children with nocturnal enuresis.
Yılören Tanıdır, Çağrı Akın Şekerci, Tuncay Top, Farhad Talibzade, Ahmet Şahan, Tarık Emre Şener, Tufan Tarcan, Ferruh Şimşek, Cem Akbal   +8 more
doaj   +1 more source

Personality Attributes of Secondary Nocturnal Enuresis Using Exner's Rorschach Comprehensive System [PDF]

Maǧallaẗ Al-I'ršād Al-Nafsī, 2015
This study investigated Rorschach Inkblot Test response patterns in a group of children diagnosed with secondary nocturnal enuresis and compared them to normal group. The mean age was 13.9.
Asmaa Othman Diab Abd-Elmaksoud
doaj   +1 more source