Results 1 to 10 of about 16,006 (225)
Indian Journal of Plastic Surgery, 2014 The term orbital hypertelorism (ORH) implies “widely apart orbits.” This may also be associated with the abnormal vertical orientation of the orbits (dystopia).
Ramesh K. Sharma
exaly +5 more sources
miR-383-3p and miR-6951-3p activate cell proliferation through the regulation of genes related to hypertelorism [PDF]
Frontiers in Cell and Developmental BiologyHypertelorism, characterized by an abnormal increase in the distance between the eyes, is often associated with various congenital birth defects. While there is increasing evidence suggesting common underlying mechanisms for hypertelorism, the role of ...
Chihiro Iwaya +2 more
doaj +2 more sources
Challenges in nasal reconstruction for facial clefts Tessier 3 bilateral and Tessier 0: a staged surgical approach case report [PDF]
Maxillofacial Plastic and Reconstructive SurgeryBackground Craniofacial anomalies, particularly Tessier facial clefts, present significant surgical and functional challenges. Bilateral Tessier 3 and Tessier 0 clefts are extremely rare, often requiring complex reconstructive strategies.
Arif Tri Prasetyo
doaj +2 more sources
Prevalence and characteristics of pediatric hypertelorism: insights from Ugwolawo, Kogi State, Nigeria [PDF]
Novelty in Clinical Medicine, 2023 Background: Hypertelorism is a medical condition characterized by an abnormally increased distance between two organs or structures, particularly the eyes.Objectives: The study aims to investigate the prevalence and characteristics of hypertelorism among
Nathaniel Ohiemi Amedu +3 more
doaj +1 more source
Citation: 'hypertelorism' in the IUPAC Compendium of Chemical Terminology, 5th ed.; International Union of Pure and Applied Chemistry; 2025. Online version 5.0.0, 2025. 10.1351/goldbook.10827 • License: The IUPAC Gold Book is licensed under Creative Commons Attribution-ShareAlike CC BY-SA 4.0 International for individual terms.
Tripathy K, Ghosh D.
europepmc +2 more sources
Oro-facial-digital syndrome: Unspecified type with the spontaneous fusion of cleft palate
Contemporary Clinical Dentistry, 2021 Oro-facial-digital syndrome (OFD) is a disorder with varied inheritance patterns. They deal mainly with abnormalities of the face, digits, i.e., fingers and toes, and oral cavity.
Prashant Kumar Verma, Nowneet Kumar Bhat
doaj +1 more source
Apert's syndrome: A rare craniofacial disorder
Journal of Indian Society of Pedodontics and Preventive Dentistry, 2020 Apert's syndrome (AS) which is a rare congenital disorder is a form of acrocephalosyndactyly. This syndrome is characterized by craniosynostosis, midface hypoplasia, and syndactyly of hands and feet.
Prajakta C Khelkar +3 more
doaj +1 more source
Frontiers in Genetics, 2023 Craniofrontonasal Syndrome is a very rare dominant X-linked genetic disorder characterized by symptoms such as hypertelorism, craniosynostosis, eye alterations, bifid nose tip, and longitudinal ridging and splitting of nails.
Harry Pachajoa +4 more
doaj +1 more source
Orbital box osteotomy in frontonasal dysplasia with severe hypertelorism: Our first experience
Journal of Cleft Lip Palate and Craniofacial Anomalies, 2023 Frontonasal dysplasia (FND) is a rare craniofacial deformity, including severe hypertelorism. We herein presented the case of a 6-year-old female patient with FND and Grade III hypertelorism who underwent a four-wall-orbital box osteotomy with a ...
I Made Suka Adnyana +2 more
doaj +1 more source
Craniofrontonasal dysplasia: A case report
Pediatric Discovery, 2023 Craniofrontonasal dysplasia (CFND) is a rare congenital malformation, which has a wide array of symptoms that can vary drastically between patients. These include coronal synostosis with associated brachycephaly, hypertelorism, cleft lip and palate, and ...
Kanad Ghosh +4 more
doaj +1 more source