Results 31 to 40 of about 27,436 (251)

Prevalence and Distribution of Nonsyndromic Dental Anomalies in Children in Eastern Saudi Arabia: A Radiographic Study

The Scientific World Journal, 2021
Objectives. To report the prevalence and distribution of nonsyndromic dental anomalies in children in eastern Saudi Arabia. Methods. This retrospective records review study involved radiographic examination of 6–18 years old pediatric patients who ...
Eman A. Bakhurji, Fatima Aldossary, Jood Aljarbo, Fatimah AlMuhammadi, Maysaa Alghamdi, Muhammad Ashraf Nazir   +5 more
doaj   +1 more source

EVALUATION OF DENTAL ANOMALY PREVELANCE AND TYPES BY CONE BEAM COMPUTED TOMOGRAPHY IN A SUBGROUP OF TURKISH POPULATİON [PDF]

Journal of Oral Health and Oral Epidemiology
Background: This study aimed to investigate the frequency and variation of dental malformations in a subgroup of the Turkish population.Methods: Cone beam computed tomography (CBCT) images taken for various reasons were scanned retrospectively.
Rumeysa Sendisci GOK, Hümeyra Tercanlı ALkış   +1 more
doaj   +1 more source

Prevalence of dental anomalies in pediatric patients at Dental and Oral Hospital of Universitas Muhammadiyah Yogyakarta

Dental Journal, 2023
Background: A dental abnormality is a deviation from the normal shape and structure of the teeth due to interference during growth and development.
Laelia Dwi Anggraini, Denna Idryareza Augustyana, Nurrofi Sekarjati   +2 more
doaj   +1 more source

Prevalence of Dental Anomalies in Orthodontic Patients

Česká Stomatologie a Praktické Zubní Lékařství, 2013
Aim: The aim of the present study was to assess the prevalence of dental anomalies and associations among them in Czech orthodontic patients and to verify possible association between the prevalence of dental anomalies and gender.
P. Černochová, L. Izakovičová Hollá
doaj   +1 more source

Variability, asymmetry and sexual dimorphism in craniofacial anomalies in Loeys-Dietz syndrome 2: geometric morphometric analysis in mice

Scientific Reports
Loeys-Dietz syndrome is a rare connective tissue disorder characterized by life-threatening aortic aneurysm and distinctive craniofacial anomalies. It is caused by mutations along the transforming growth factor beta (TGF-β) signaling pathway (LDS1-6). We
Katelin R. Devine, Sarah Lynn, Priyam Jani, Cyrus Keyvanfar, Bikash Lamichhane, Ashleigh S. Hanner, Catharine Dietrich, Rachel S. Chung, Pamela A. Frischmeyer-Guerrerio, Konstantinia Almpani, Olivier Duverger, Janice S. Lee   +11 more
doaj   +1 more source

Streamlining Diagnosis of Bardet–Biedl Syndrome: New Diagnostic Algorithm With Updated Criteria

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Considerable advances have been made in our understanding of Bardet–Biedl syndrome (BBS), particularly in its core clinical features and molecular genetics, warranting an update to the existing diagnostic criteria framework. Using a rigorous, evidence‐based, and consensus‐driven process, a multidisciplinary group of international experts and ...
Jeremy J. Pomeroy, Jesse Richards, Brooke R. Sweeney, Seema Kumar, Katie E. Queen, Joshua Zaritsky, Carl H. Cramer, Elias I. Traboulsi, Brittni A. Scruggs, Erica E. Davis, Ekaterina Keifer, Emma McGibbon, Timothy Ogden, Bendert De Graaf, Tonia Hymers, Elizabeth Forsythe, Philip Beales   +16 more
wiley   +1 more source

Acute hyperlipidemia has transient effects on large-scale bone regeneration in male mice

Scientific Reports
Excessive dietary fat intake increases plasma lipid levels and has been associated with reduced bone mineral density (BMD) and increased risk of osteoporotic fracture, especially in older postmenopausal women.
Luciana Yamamoto de Almeida, Catharine Dietrich, Olivier Duverger, Janice S. Lee   +3 more
doaj   +1 more source

De Novo 2.2 Mb 19q13.42–q13.43 Microdeletion Encompassing U2AF2: Support for a Haploinsufficiency Model

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT U2 small nuclear RNA auxiliary factor 2 (U2AF2) is an essential pre‐mRNA splicing factor involved in the early stages of pre‐mRNA splicing. To date, multiple individuals have been reported with predominantly heterozygous missense variants presenting intellectual disability, speech and motor delays, seizures, hypotonia, and thin or hypoplastic ...
Amanda Toledo, Sarah Araji, Weimin Bi, Seema R. Lalani   +3 more
wiley   +1 more source

Histidine Supplementation Stabilizes Hearing and Vision and Improves Growth in HARS1‐Related Autosomal Recessive Disorder Associated With Usher‐Like Symptoms

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Autosomal recessive HARS1‐related disorder (originally described as Usher syndrome type 3B) caused by a homozygous Y454S variant in the histidyl‐tRNA synthetase gene (HARS1) is characterized by progressive sensorineural hearing and vision loss and respiratory deterioration with risk for sudden death following febrile illnesses.
Victoria Mok Siu, Rosan Kenana, Rana Chakrabarti, Sarah D. P. Wilhelm, Joseph Andrews, Susan J. Leat, Christina Parker, Michael Miller, Leslie A. Nangle, Wendy McCaul, Ashfia Chowdhury, Natalie Hutchings, Ryan A. Adams, Lauren Guy, Mandy Rhody, Verena Juncal, Marisa I. Mendes, Desiree E. C. Smith, Gajja S. Salomons, Angelica A. Moresco, Daphne L. McCulloch, D. Holmes Morton, Ilka U. Heinemann, C. Anthony Rupar   +23 more
wiley   +1 more source

Prevalence of Dental Anomalies Among the Pediatric Population at Abbasi Shaheed Hospital, Karachi, Pakistan: A Cross-Sectional Survey [PDF]

The International Journal of Frontier Sciences
Background: Pediatric dental anomalies refer to irregularities or abnormalities in the development, structure, or positioning of the teeth in the oral cavity of children.
Maryam Zafar, Aiman Shaikh, Maliha Mohsin   +2 more
doaj   +1 more source