Results 31 to 40 of about 5,272 (228)

Cosmetic Lateral Canthoplasty: Lateral Canthoplasty to Lengthen the Lateral Canthal Angle and Correct the Outer Tail of the Eye

Archives of Plastic Surgery, 2016
There are many women who want larger and brighter eyes that will give a favorable impression. Surgical methods that make the eye larger and brighter include double eyelidplasty, epicanthoplasty, as well as lateral canthoplasty.
Soo Wook Chae, Byung Min Yun
doaj   +1 more source

Simplifying Diagnosis of Fetal Alcohol Syndrome Using Machine Learning Methods

Frontiers in Pediatrics, 2022
IntroductionThe fetal alcohol spectrum disorder (FASD) is a complex and heterogeneous disorder, caused by gestational exposure to alcohol. Patients with fetal alcohol syndrome (FAS—most severe form of FASD) show abnormal facial features.
Moritz Blanck-Lubarsch, Dieter Dirksen, Reinhold Feldmann, Eike Bormann, Ariane Hohoff   +4 more
doaj   +1 more source

Palpebral fissure widening after different types of strabismus surgery

Academic Journal of Health Sciences, 2022
[spa] Objetivos: La cirugía de estrabismo puede estar asociada a complicaciones postquirúrgicas como el ensanchamiento de la fisura palpebral. Para una mejor comprensión de este hallazgo, estudiamos el resultado quirúrgico de los pacientes sometidos a cirugía de estrabismo en nuestro centro y su efecto sobre las alteraciones de la fisura ...
Medghalchi, Abdolreza, Akbari, Mitra, Soltani Moghadam, Reza, Alizadeh, Yousef, Kazemnejad, Ehsan, Fatemeh Mirjani, Seyedeh, Atakpour, Farhad   +6 more
openaire   +2 more sources

Reoperation of strabismus, points to be considered

Journal of the Egyptian Ophthalmological Society, 2018
Purpose The aim was to obtain the best results when dealing with previously operated cases of strabismus, as regards the restoration of ocular alignment, regaining ocular motility at least in the central field and at the same time aiming at preserving ...
Karim A Gaballah
doaj   +1 more source

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

American Journal of Medical Genetics Part A, EarlyView.
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

Non‐RASopathy Genetic Syndromes Identified as the Molecular Cause of Disease in Patients Previously Diagnosed With Noonan Syndrome

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Noonan Syndrome (NS) is a clinically and genetically heterogeneous condition characterized by typical facial dysmorphisms, short stature, congenital heart defects, and developmental delays. While variants in genes such as PTPN11, SOS1, and RAF1 account for most genetically confirmed cases, diagnosis is challenging due to phenotypic overlap ...
Gabriela Jeesoo Kim, Alexsandra Christianne Malaquias, Debora Romeo Bertola, Raissa Carneiro Rezende, Laurana De Polli Cellin, Lucas Vieira Lacerda Pires, Ana Maria Santillan‐Vasconez, Antônio Marcondes Lerario, Renata da Cunha Scalco, Alexander Augusto de Lima Jorge   +9 more
wiley   +1 more source

Tarsal switch using an anterior approach to correct severe ptosis

Archives of Plastic Surgery, 2018
Background To present the outcomes of the tarsal switch procedure using an anterior approach to correct severe ptosis with poor levator muscle function (
Roberta Lilian Fernandes de Sousa Meneghim, Lucieni Barbarini Ferraz, Alicia Galindo-Ferreiro, Rajiv Khandekar, Hortensia Sanchez-Tocino, Silvana Schellini   +5 more
doaj   +1 more source

Genotypes and Phenotypes of Patients With TSPEAR‐Related Disorder: Evidence of a Predominant Dental Phenotype

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT TSPEAR (chr. 21q22.3) encodes a protein involved in tooth development and is predominantly expressed in the enamel knot. Biallelic loss of function variants in TSPEAR cause ectodermal dysplasia, tooth agenesis and sensorineural hearing loss. However, the role of TSPEAR in auditory processes is unclear.
Debora Vergani, Lucia Tiberi, Annarita Giliberti, Elia Dirupo, Laila Zaroili, Francesco Brancati, Michela Brena, Stefano Caraffi, Chiara De Luca, Livia Garavelli, Anna Virginia Gulino, Milena Mariani, Marzia Pollazzon, Angelo Selicorni, Samuela Landini, Ilaria Sani, Rosangela Artuso, Angela Peron   +17 more
wiley   +1 more source

Duane retraction syndrome in a Nigerian child

The Pan African Medical Journal, 2014
We report a case of a four year old Nigerian girl who presented to the paediatric unit of our eye clinic with complaints of a squint on looking to the right side and reduction in the size of the right eye when looking to the left. On examination, she had
Olusola Oluyinka Olawoye, Bolutife Ayokunnu Olusanya, Aderonke Mojisola Baiyeroju   +2 more
doaj   +1 more source

The Diagnosis That Arrived Decades Late: Living Without and Then With Myhre Syndrome

American Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Myhre syndrome (MIM #139210) is a rare multisystem disorder first described in 1981, characterized by short stature, neurodevelopmental delay, joint contractures, and cardiopulmonary complications. Its molecular basis, recurrent pathogenic variants in SMAD4, was not discovered until 2011. This narrative is based on a review of medical records,
Abdallah F. Elias
wiley   +1 more source