Results 61 to 70 of about 3,765 (196)

Comparative Evaluation of Sella Turcica Morphology and Dimensions in Skeletal Class III Malocclusion and Cleft Lip and Palate Patients Versus Class I Individuals

Clinical and Experimental Dental Research, Volume 12, Issue 2, April 2026.
ABSTRACT Objectives To compare the morphology and dimensions of the sella turcica in skeletal Class III malocclusion and cleft lip and palate (CLP) with Class I. Material and Methods This comparative cross‐sectional study was conducted at the Armed Forces Institute of Dentistry, Rawalpindi, Pakistan, and involved 540 cases (Class I, Class III ...
Bushra Gul, Erum Amin, Umar Hussain, Faiza Malik, Rana Faiza, Sundus Saad Alqarni, Waqas Naseem   +6 more
wiley   +1 more source

Correlation of RUNX2 Variants With Craniofacial–Dental Phenotypes in Cleidocranial Dysplasia

Clinical and Experimental Dental Research, Volume 12, Issue 2, April 2026.
ABSTRACT Objectives Cleidocranial dysplasia (CCD) is a rare RUNX2‐related skeletal disorder characterized by craniofacial anomalies and skeletal Class III malocclusion. However, the relationship between RUNX2 variant type and phenotype severity remains unclear. This study aimed to evaluate the association between RUNX2 variant types and the severity of
Pintu‐on Chantarawaratit, Sermporn Thaweesapphithak, Pisha Pittayapat, Thantrira Porntaveetus   +3 more
wiley   +1 more source

Tongue and Hyoid Bone Positions and Its Relations to the Mandibular Anterior Teeth: A Cone‐Beam Computed Tomography Study

Orthodontics &Craniofacial Research, Volume 29, Issue 2, Page 247-257, April 2026.
ABSTRACT Objectives This study aimed to investigate the position of the tongue and hyoid bone at rest according to incisal relationships using cone beam computed tomography and to examine whether dentoskeletal measurements are correlated with these positions.
Hieu Nguyen, Ji‐Hye Park, Till Edward Bechtold, Jung Jin Park, Yoon Jeong Choi   +4 more
wiley   +1 more source

Growth Standards for Children With Smith–Magenis Syndrome (SMS)

American Journal of Medical Genetics Part A, Volume 200, Issue 3, Page 569-578, March 2026.
ABSTRACT Smith–Magenis syndrome (SMS, OMIM 182290) is a complex syndromic diagnosis marked by neurobehavioral differences and distinct facial dysmorphisms, caused by haploinsufficiency of the retinoic acid‐1 (RAI1) gene either by a pathogenic sequence variant or deletion at chromosome 17p11.2 involving a portion or all of this gene.
Julie Hoover‐Fong, John McGready, Leah Fleming, Kerry Schulze, Folami Duncan, Alexis Leonard, Marie Christine de Blois Boucard, Danilo Moretti‐Ferreira, Andrea L. Gropman, Wendy J. Introne, Ann C. M. Smith   +10 more
wiley   +1 more source

Nance‐Horan Syndrome: Further Delineation of the Affected Male and the Female Carrier Phenotypes

American Journal of Medical Genetics Part A, Volume 200, Issue 3, Page 642-652, March 2026.
ABSTRACT Nance‐Horan syndrome (NHS; OMIM 302350) is a rare, X‐linked syndrome characterized by bilateral congenital cataracts leading to profound vision loss, specific dental anomalies including characteristic screwdriver blade‐shaped incisors, facial anomalies, and intellectual disability.
Maria K. Haanpää, Chad R. Haldeman‐Englert, Marja Hietala, Melisa S. Tanverdi, Patrick P. Koty, Diana Brightman, Eniolami Dosunmu, Shailja Tibrewal, Savleen Kaur, Anupriya Kaur, Raj Kumar Verma, Alejandra G. de Alba Campomanes, Virginia Utz, Anne M. Slavotinek, Cynthia Curry   +14 more
wiley   +1 more source

Genioplasty and vestibuloplasty of edentulous mandibular prognathism patient

, 2002
P(論文)This report describes a case of mandibular prognathism with edentulous jaw. The patient was a 56-year-old female who had nonconformance of the complete denture and protrusion of the lower jaw.
37470, 金澤, 正昭, 37471, 37472, 37473, 茂尾, 公晴, 37474, 37475, 武藤, 壽孝, 江上, 史倫, 越野, 寿, 26354, 萩野, 司, 37469, 平井, 敏晴, 山本, 圭子   +15 more
core  

The Identification of a Novel Locus for Mandibular Prognathism in the Han Chinese Population

, 2010
Mandibular prognathism is a common dentofacial phenotype with a substantial genetic component; however, few susceptibility loci have been mapped. Ethnicity is a risk factor for mandibular prognathism, and a relatively high prevalence is observed in ...
F. Chen, F. Zhang, Q. Li, X. Li
core   +1 more source

Effect of the rs7858836 Single‐Nucleotide Polymorphisms of the ASTN2 Gene on Pain‐Related Phenotypes in Japanese Women Who Underwent Laparoscopic Gynecologic Surgery

Neuropsychopharmacology Reports, Volume 46, Issue 1, March 2026.
Schematic overview of the study examining the association between the ASTN2 rs7858836 T allele and postoperative pain–related phenotypes in humans. The analysis focuses on the relationship between this genetic variant and postoperative pain intensity as well as analgesic responses.
Rie Inoue, Daisuke Nishizawa, Shoko Okahara, Atsuko Hara, Hisako Okada, Junko Hasegawa, Yuko Ebata, Kyoko Nakayama, Masakazu Hayashida, Kazutaka Ikeda   +9 more
wiley   +1 more source

The effects of sagittal ramus osteotomy for mandibular prognathism on maximum mouth opening and condylar movement

, 1997
P(論文)Maximum mouth opening and condylar movement before and more than 6 months after surgery were analyzed in 23 cases of sagittal ramus osteotomy of the mandible for correction of mandibular prognathism.
KAWAKAMI, Johji, 37970, 37971, YAMAGUCHI, Nobuhito, UCHIDA, Nobuhiko, KOBAYASHI, Hiroki, 37972, YOKOYAMA, Kazunori, 37973, Toshitaka, MUTO, 37974, 37975, 37976, 37977, 37978, 37979, 37980, 37981, 37982, 25279, MUTO, Toshitaka, KOKUBO, Yukihiro, 37969, 37983, YAMAZAKI, Atsue, 37984, 37985, 37986, 37987, KANAZAWA, Masaaki, 37967, UGA, Shigeru, 37968, ISHII, Hideshi   +33 more
core  

Shaping the human face: Periosteal bone modeling across ontogeny

The Anatomical Record, Volume 309, Issue 2, Page 271-292, February 2026.
Abstract Facial morphology is a defining aspect of Homo sapiens that distinguishes our species from fossil ancestors and plays a central role in estimating age, sex, and ancestry in both past and present populations. Understanding how the face develops during postnatal ontogeny is essential for interpreting adult facial variation.
Sarah E. Freidline, Madison Hubbart, Catherine Shipman, Najielie Burgos, Chiara Villa, Alexandra Schuh   +5 more
wiley   +1 more source