AimsTo assess the rates of incontinence and associated psychological problems in children, adolescents and adults with Down Syndrome, a genetic syndrome caused by partial or complete triplication (trisomy) of chromosome 21 and characterized by typical facial features, a physical growth delay and mild or moderate intellectual disability.MethodsThree hundred and seventeen persons with Down Syndrome (4-51 years) were recruited through a German parent support group (59.6% male, mean age 19.2 years). The Parental Questionnaire: Enuresis/Urinary Incontinence, the Incontinence Questionnaire-Pediatric Lower Urinary Tract Symptoms, as well as the Developmental Behavior Checklist (DBC) for parents or for adults were filled out by parents or care-give...
Fragile-X-syndrome (FXS) is caused by a mutation on the X chromosome (Xq27.3). Males with a full mut...
OBJECTIVE To assess and identify the frequency and type of urinary incontinence (UI), as well as ass...
Background: Mowat-Wilson Syndrome (MWS) is caused by deletion/mutation of the ZEB2 gene on chromosom...
AimsTo assess the rates of incontinence and associated psychological problems in children, adolescen...
Aims Williams Syndrome (WS) is a microdeletion syndrome (chromosome 7q11.23) characterized by typica...
ObjectiveNoonan Syndrome (NS) is an autosomal neuro-developmental disorder with a high phenotypic va...
Lower urinary tract dysfunction (LUTD) is a common problem in children. Data on it's prevalence in i...
PURPOSE: Children with Down syndrome (DS) are more likely to experience bladder bowel dysfunctio...
Aims In children with Down syndrome (DS) which causes cognitive impairment and intellectual disabili...
OBJECTIVE: To assess problem behavior in adolescents with Down syndrome and examine the association ...
To examine the prevalence of medical conditions and use of health services among young adults with D...
Angelman syndrome (AS) is a congenital syndrome with a prevalence of 1:15,000. Individuals with AS o...
Introduction Fetal alcohol spectrum disorders (FASD) are one of the leading preventable causes of in...
Background Despite the fact that functional lower urinary tract symptoms are common among people wit...
Objective: To examine the prevalence of medical conditions and use of health services among young ad...
Fragile-X-syndrome (FXS) is caused by a mutation on the X chromosome (Xq27.3). Males with a full mut...
OBJECTIVE To assess and identify the frequency and type of urinary incontinence (UI), as well as ass...
Background: Mowat-Wilson Syndrome (MWS) is caused by deletion/mutation of the ZEB2 gene on chromosom...
AimsTo assess the rates of incontinence and associated psychological problems in children, adolescen...
Aims Williams Syndrome (WS) is a microdeletion syndrome (chromosome 7q11.23) characterized by typica...
ObjectiveNoonan Syndrome (NS) is an autosomal neuro-developmental disorder with a high phenotypic va...
Lower urinary tract dysfunction (LUTD) is a common problem in children. Data on it's prevalence in i...
PURPOSE: Children with Down syndrome (DS) are more likely to experience bladder bowel dysfunctio...
Aims In children with Down syndrome (DS) which causes cognitive impairment and intellectual disabili...
OBJECTIVE: To assess problem behavior in adolescents with Down syndrome and examine the association ...
To examine the prevalence of medical conditions and use of health services among young adults with D...
Angelman syndrome (AS) is a congenital syndrome with a prevalence of 1:15,000. Individuals with AS o...
Introduction Fetal alcohol spectrum disorders (FASD) are one of the leading preventable causes of in...
Background Despite the fact that functional lower urinary tract symptoms are common among people wit...
Objective: To examine the prevalence of medical conditions and use of health services among young ad...
Fragile-X-syndrome (FXS) is caused by a mutation on the X chromosome (Xq27.3). Males with a full mut...
OBJECTIVE To assess and identify the frequency and type of urinary incontinence (UI), as well as ass...
Background: Mowat-Wilson Syndrome (MWS) is caused by deletion/mutation of the ZEB2 gene on chromosom...