Results 21 to 30 of about 7,360,727 (379)

1p36 Deletion Syndrome and the Aorta: A Report of Three New Patients and a Literature Review

Journal of Cardiovascular Development and Disease, 2021
Background: Monosomy 1p36 syndrome is now considered the most common terminal deletion syndrome, with an estimated incidence of 1 in 5000. Cardiac involvement is well described in the literature mainly in terms of congenital heart defects (CHDs) and ...
Valentina Lodato, Valeria Orlando, Viola Alesi, Silvia Di Tommaso, Mario Bengala, Giovanni Parlapiano, Elisa Agnolucci, Marianna Cicenia, Federica Calì, Maria Cristina Digilio, Fabrizio Drago, Antonio Novelli, Anwar Baban   +12 more
doaj   +1 more source

Cardiomyopathies in Children and Systemic Disorders When Is It Useful to Look beyond the Heart?

Journal of Cardiovascular Development and Disease, 2022
Cardiomyopathy (CMP) is a rare disease in the pediatric population, with a high risk of morbidity and mortality. The genetic etiology of CMPs in children is extremely heterogenous.
Valentina Lodato, Giovanni Parlapiano, Federica Calì, Massimo Stefano Silvetti, Rachele Adorisio, Michela Armando, May El Hachem, Antonino Romanzo, Carlo Dionisi-Vici, Maria Cristina Digilio, Antonio Novelli, Fabrizio Drago, Massimiliano Raponi, Anwar Baban   +13 more
doaj   +1 more source

Global prevalence of autism: A systematic review update

Autism Research, 2022
Prevalence estimates of autism are essential for informing public policy, raising awareness, and developing research priorities. Using a systematic review, we synthesized estimates of the prevalence of autism worldwide. We examined factors accounting for
Jinan Zeidan, E. Fombonne, Julie Scorah, Alaa Ibrahim, M. Durkin, S. Saxena, A. Yusuf, A. Shih, M. Elsabbagh   +8 more
semanticscholar   +1 more source

Prevalence of Postpartum Family Planning Service Coverage in Selected Referral Facilities of Nepal [PDF]

, 2020
Introduction: Nepal Society of Obstetricians and Gynecologists jointly with the Nepalese government and with the support from the International Federation of Obstetrics and Gynecology has implemented an initiative to institutionalize postpartum family ...
Acharya, S, Arulkumaran, S, Dhital, R, Makins, A, Mishra, S, Pokhrel, S, Pokhrel, SM, Poudel, A, Rajbhandari, S, Singh, D, Subedi, S, Thapa, K, Thapa, K, Thapa, S, Tunnacliffe, E-A, Vaidya, S   +15 more
core   +1 more source

Geno- and phenotypic characteristics and clinical outcomes of CACNA1C gene mutation associated Timothy syndrome, “cardiac only” Timothy syndrome and isolated long QT syndrome 8: A systematic review

Frontiers in Cardiovascular Medicine, 2022
BackgroundMutations in the CACNA1C gene–encoding for the major Ca2+ channel of the heart–may exhibit a variety of clinical manifestations. These include typical or atypical Timothy syndromes (TS) which are associated with multiple organ manifestations ...
János Borbás, Máté Vámos, Lidia Hategan, Lilla Hanák, Nelli Farkas, Zsolt Szakács, Zsolt Szakács, Dezső Csupor, Dezső Csupor, Bálint Tél, Péter Kupó, Péter Kupó, Beáta Csányi, Viktória Nagy, András Komócsi, Tamás Habon, Tamás Habon, Péter Hegyi, Péter Hegyi, Péter Hegyi, Róbert Sepp   +20 more
doaj   +1 more source

Global Prevalence of Depressive and Anxiety Symptoms in Children and Adolescents During COVID-19: A Meta-analysis.

JAMA pediatrics, 2021
Importance Emerging research suggests that the global prevalence of child and adolescent mental illness has increased considerably during COVID-19.
N. Racine, B. McArthur, J. Cooke, Rachel Eirich, Jenney Zhu, S. Madigan   +5 more
semanticscholar   +1 more source

Myocardial and Arrhythmic Spectrum of Neuromuscular Disorders in Children

Biomolecules, 2021
Neuromuscular disorders (NMDs) are highly heterogenous from both an etiological and clinical point of view. Their signs and symptoms are often multisystemic, with frequent cardiac involvement.
Anwar Baban, Valentina Lodato, Giovanni Parlapiano, Corrado di Mambro, Rachele Adorisio, Enrico Silvio Bertini, Carlo Dionisi-Vici, Fabrizio Drago, Diego Martinelli   +8 more
doaj   +1 more source

Cardiovascular Involvement in Pediatric Laminopathies. Report of Six Patients and Literature Revision

Frontiers in Pediatrics, 2020
Lamin A/C (LMNA) encodes for two nuclear intermediate filament proteins. Mutations in LMNA cause a highly heterogeneous group of diseases predominantly leading to muscular or cardiac disease, lipodystrophy syndromes, peripheral neuropathy, and ...
Anwar Baban, Marianna Cicenia, Monia Magliozzi, Maria Gnazzo, Nicoletta Cantarutti, Massimo Stefano Silvetti, Rachele Adorisio, Bruno Dallapiccola, Enrico Bertini, Antonio Novelli, Fabrizio Drago   +10 more
doaj   +1 more source

Prevalence of Autism Spectrum Disorder Among Children Aged 8 Years — Autism and Developmental Disabilities Monitoring Network, 11 Sites, United States, 2016

Morbidity and mortality weekly report. Surveillance summaries, 2020
Problem/Condition Autism spectrum disorder (ASD). Period Covered 2016. Description of System The Autism and Developmental Disabilities Monitoring (ADDM) Network is an active surveillance program that provides estimates of the prevalence of ASD among ...
M. Maenner, K. Shaw, J. Baio, Anita Washington, Mary E. Patrick, M. Dirienzo, D. Christensen, L. Wiggins, S. Pettygrove, J. Andrews, M. Lopez, Allison Hudson, Thaer M Baroud, Yvette D. Schwenk, Tiffany White, C. Rosenberg, L. Lee, R. Harrington, M. Huston, A. Hewitt, A. Esler, J. Hall-Lande, J. Poynter, Libby Hallas-Muchow, J. Constantino, Robert T. Fitzgerald, W. Zahorodny, Josephine Shenouda, J. Daniels, Z. Warren, Alison C. Vehorn, Angelica Salinas, M. Durkin, P. Dietz   +33 more
semanticscholar   +1 more source

Global Prevalence of Prediabetes.

Diabetes Care, 2023
OBJECTIVE To estimate the global, regional, and national prevalence of prediabetes, defined by impaired glucose tolerance (IGT) or impaired fasting glucose (IFG).
M. Rooney, Michael Fang, K. Ogurtsova, Bige Ozkan, J. Echouffo-Tcheugui, E. Boyko, D. Magliano, E. Selvin   +7 more
semanticscholar   +1 more source