Results 71 to 80 of about 260,204 (307)

Phenotype Expansion of Malan Syndrome: New Cases and a Review of the Literature

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Malan syndrome is an ultra‐rare overgrowth syndrome caused by pathogenic variants or deletions in nuclear factor one X (NFIX) located at 19p13.2. Here, we report a comprehensive literature review and phenotyping of known patients with Malan syndrome and present a novel cohort of eight patients.
Alex F. Nisbet, Sylvie A. Adams, Zoe S. Katz, Christal G. Delagrammatikas, Kosuke Izumi, Winifred Sigal, Kim Ventarola, Elaine H. Zackai, Julia E. Reid, Grant T. Liu, Jennifer M. Kalish   +10 more
wiley   +1 more source

Effectiveness of parenting based on organizational skills on symptoms of children with attention deficit hyperactivity disorder

Taḥqīqāt-i ̒Ulūm-i Raftārī, 2021
Aim and Background: The aim of this study was to investigate the effectiveness of parenting based on organizational skills on symptoms of students with attention deficit hyperactivity disorder.
Abdolhossein Shamsi, Amir Ghamarani
doaj  

Occupational therapy for children with attention deficit hyperactivity disorder (ADHD), Part 1: A delineation model of practice [PDF]

, 2007
In the United Kingdom (UK), occupational therapy for children with attention deficit hyperactivity disorder (ADHD) is a small field of practice (Chu 2003a), even though 5% of school-aged children in the population are affected by the condition ...
Reynolds, F
core   +1 more source

High‐Resolution Genomic Characterization of WAGR Spectrum Disorder: Insights From a Novel Cohort and Literature Synthesis, and Validation of Patient‐Reported Data

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT WAGR spectrum disorder (WAGRSD) is an ultra‐rare congenital disorder caused by heterozygous deletion of chromosome 11p13. While classically associated with Wilms tumor, Aniridia, Genitourinary anomalies, and a Range of developmental delays, accurate delineation of the deletion is critical for prognosis because the phenotypic spectrum extends ...
Andrew M. George, Bamelak T. Duki, Zoe S. Katz, Aravind Viswanathan, Suzanne P. MacFarland, Evan R. Hathaway, Caitlin Monahan, John Morris, Kelly L. Trout, Shari M. Krantz, Arupa Ganguly, Jennifer M. Kalish   +11 more
wiley   +1 more source

Attention Deficit HyperactivityDisorder (ADHD): Survey Report [PDF]

, 2017
In the spring of 2016, the New Hampshire Pediatric Improvement Partnership (NHPIP) conducted an online survey of NH pediatric and family practice clinicians to understand practice patterns, comfort level, and support needs relative to caring for ...
Daviss, W. Burl, House, Samantha, Olson, Ardis, O’Neil, Molly, Porter, Josephine, Ryer, Jeanne, EdD, Tutko, Holly Deblois   +6 more
core   +1 more source

Clinical, Behavioral and Neuroradiological Phenotype in an Italian Cohort of Patients With Xia Gibbs Syndrome: A Multicenter Cross‐Sectional Study and Systematic Literature Review

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Heterozygous variants in the AHDC1 gene are associated with Xia Gibbs Syndrome (XGS), a genetic disorder with a highly variable phenotype. Cognitive impairment, motor delay, language delay, neonatal hypotonia, and sleep apnea are considered “cardinal” signs of the disease.
Giulia Cinelli, Stefania Della Vecchia, Patrizia Bergonzini, Elisa Caramaschi, Elisabetta Spezia, Claudia Parenti, Simona Filomena Madeo, Laura Lucaccioni, Cavalleri Francesca, Marisa Pugliese, Federico Raviglione, Clara Colonna, Olga Calabrese, Ilaria Stanghellini, Maria Carmen Marongiu, Enrico Biagioni, Anna Rita Ferrari, Roberta Battini, Lorenzo Iughetti   +18 more
wiley   +1 more source

Digital Inclusion for Students with Attention Deficit Hyperactivity Disorder [PDF]

, 2018
The Attention Deficit Hyperactivity Disorder is a syndrome characterized by distraction, impulsivity, forgetfulness and disorganization. The diagnosis requires considerable care and experience.
Mata, D. C. (Dayane), Oliveira, G. R. (Gilmara), Oliveira, J. C. (João)   +2 more
core  

The effects of stimulants on eating patterns in children and adolescents with Attention Deficit Hyperactivity Disorder [PDF]

, 2019
Objectives. This study aims to evaluate the effects of methylphenidate (MPH) on eating patterns and body mass index (BMI) in children with attention deficit/hyperactivity disorder (ADHD).
Akay, Aynur Pekcanlar, Turan, Serkan
core   +4 more sources

Patient Perspectives on Psychiatric Polygenic Risk Scores in Reproductive Decision‐Making and Polygenic Embryo Screening

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, EarlyView.
ABSTRACT Polygenic risk scores (PRS) estimate individuals' genetic risk for developing multifactorial conditions. Recent genome‐wide association studies have enabled development of psychiatric PRS, which hold potential to streamline diagnosis and treatment of psychiatric conditions.
Lauren A. Ginn, Amanda R. Merner, Page M. Trotter, Kaitlynn P. Craig, Abigail C. Martinez, Ana Lucía Battaglino, Dorit Barlevy, Daphne M. Ayton, Takahiro Soda, Eric A. Storch, Gabriel Lázaro‐Muñoz, Stacey Pereira   +11 more
wiley   +1 more source

Attention deficit hyperactivity disorder and associated factors among children and adolescents in Borama town, Somaliland: a community-based cross-sectional study

BMC Psychiatry
Background Attention deficit hyperactivity disorder is a neurodevelopmental disorder marked by a persistent pattern of symptoms, including inattention, hyperactivity, and impulsivity. Children and adolescents with attention deficit hyperactivity disorder
Mekonin Meskelu Shegere, Ahmed Moumin Abdilahi, Seid Yimam Ali, Hoodo Abdilahi Ibrahim, Amal Abdifatah Abdilahi, Abdiqani Mohamed Osman, Amiin Abdilahi Ibrahim, Fadumo Abdikarim Mohamed, Kahsay Hailu Negash   +8 more
doaj   +1 more source