Results 71 to 80 of about 272,029 (269)

Descriptive Epidemiology From the Myhre Syndrome Foundation Registry: The Value of Self‐Reported Data

American Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Myhre syndrome is an ultrarare genetic disease characterized by short stature, distinct craniofacial features, cardiovascular and respiratory fibrosis and stenosis, neurodevelopmental delays, autism, intellectual disability, and hearing loss. The natural history of Myhre syndrome is still not fully understood due to a small patient population ...
Mary K. Young, Armelle Pindon, Maggie R. Brand, Kate Wears, Katherine H. Young, Alyssa Mendel, Michael J. Lyons   +6 more
wiley   +1 more source

KDM2B‐Related Neurodevelopmental Disorder A Case‐Series Supporting the CxxC Domain Phenotype With Emphasis on Ocular and Dermatologic Features

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT The KDM2B‐related neurodevelopmental disorder is a recently identified Mendelian disorder of the epigenetic machinery associated with pathogenic variants in KDM2B. Global developmental delay, intellectual disability, congenital anomalies, and systemic manifestations characterize the disorder.
Adriana Gomes, Álvaro Martín‐Rodríguez, Miguel Del Campo, Lynne M. Bird   +3 more
wiley   +1 more source

Effect of physiotherapy interventions on attention, hyperactivity, motor and cognitive outcomes in children with attention deficit hyperactivity disorder: a systematic review protocol

Frontiers in Child and Adolescent Psychiatry
IntroductionAttention Deficit Hyperactivity Disorder (ADHD) is a prevalent neurodevelopmental disorder among children who attend school, characterized by symptoms of hyperactivity, impulsivity, and inattention.
Sakshi Desai, Sharath Hullumani, Irshad Qureshi, Rutuja Sawalkar, Aishik Ghosh   +4 more
doaj   +1 more source

Children with Attention Deficit Hyperactivity Disorder

INFAD, 2014
This article titled “Children with deficit of attention and hyperactivity in school context”, aims to inform and describe this behavioral disorder that affects children worldwide about 5.3%.
Anabela da Silva Coutinho
doaj   +1 more source

Integral intervention in a child with epilepsy and attention-deficit/hyperactivity disorder symptoms [PDF]

, 2014
A lo largo de estos años la investigación científica ha estudiado la aparición de síntomas típicos del Trastorno de Déficit de Atención con Hiperactividad en niños con epilepsia y su nivel de prevalencia.
Alonso García, Idaira María, Martínez López, María Dolores, Martínez-González, Agustín Ernesto   +2 more
core   +4 more sources

Marfan Syndrome Associated With Intellectual Disability and Behavioral Anomalies: Further Evidence for the Effect of Compound Heterozygous Variants in FBN1 on Phenotypic Severity

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Marfan syndrome (MFS) is a rare connective tissue disorder characterized by involvement of the cardiovascular, ocular, and musculoskeletal systems. Pathogenic variants in FBN1 cause most of the MFS cases; however, intellectual disability (ID) is rarely observed. A non‐consanguineous Pakistani family with four affected individuals was recruited.
Azmatullah Khan, Naseebullah Kakar, Ainullah Kakar, Malte Spielmann, Sajid Malik   +4 more
wiley   +1 more source

Household task participation of children and adolescentes with ADHD: a systematic review

Cadernos Brasileiros de Terapia Ocupacional, 2018
Introduction: In the Attention-Deficit/Hyperactivity Disorder (ADHD), the identification of functional impairments in home context is an important feature for the diagnosis.
Camila Guimarães Mendes, Marisa Cotta Mancini, Débora Marques Miranda   +2 more
doaj   +1 more source

A comprehensive investigation of memory impairment in attention deficit hyperactivity disorder and oppositional defiant disorder [PDF]

, 2012
We conducted a comprehensive and systematic assessment of memory functioning indrug-naïve boys with attention deficit hyperactivity disorder (ADHD) and oppositional defiant disorder (ODD).
Alloway, American Psychiatric Association, Baddeley, Baddeley, Baddeley, Baddeley, Barkley, Bayliss, Cannon, Castellanos, Coghill, Coghill, Cowan, Dunn, D’Esposito, Faraone, Gathercole, Gibson, Happé, Holmes, Holmes, Jarrold, Jarvis, Karatekin, Kaufman, Kempton, Kim, Kline, Klingberg, Krauel, Luciana, Martinussen, Martinussen, Matthews, Morris, Narhi, Oosterlaan, Oosterlaan, Pennington, Rhodes, Rhodes, Rhodes, Rhodes, Rubia, Scheres, Schneider, Shue, Skowronek, Swanson, Teichner, Toren, Unsworth, Van Goozen, Verte, Willcutt, Willcutt   +55 more
core   +1 more source

Neurodevelopmental and Psychiatric Studies in Children and Adolescents With Neurofibromatosis Type I: A Comprehensive Scoping Review

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, EarlyView.
ABSTRACT A comprehensive synthesis of the broad range of neurodevelopmental and psychiatric manifestations in NF1 is needed to identify knowledge gaps and future directions for NF1 research. In the following scoping review, we identify and summarize the scope of research that examines neurodevelopmental and psychiatric manifestations, both as ...
Meera Chopra, Tin‐Suet Joan Lee, Jacob Vorstman, Patricia Parkin, Louise Gallagher, Aneta Krakowski   +5 more
wiley   +1 more source

Practitioner review: pathways to care for ADHD - a systematic review of barriers and facilitators [PDF]

, 2015
Background. Attention-Deficit/Hyperactivity Disorder (ADHD) is a common neurodevelopmental disorder starting in childhood that may persist into adulthood.
Chakrabarti, I, Coates, J, Daley, D, Kochhar, P, Mills, J, Moldavsky, M, Sayal, K, Schneider, J, Sorour, W, Wright, N   +9 more
core   +2 more sources