Results 31 to 40 of about 28,866 (195)

A rare case of stickler marshall syndrome

TNOA Journal of Ophthalmic Science and Research, 2020
A 35 year old female presented to us with sudden painless diminution of vision in the right eye (RE) since 10 days. There was no history of trauma. She gave systemic history of hearing loss since 4 years of age and also complained of joint pains on and ...
Bharat Gurnani, Kirandeep Kaur
doaj   +1 more source

An Unoperated Crouzon Family Treated with Monobloc Distraction: Challenges and Lessons

Plastic and Reconstructive Surgery, Global Open, 2021
Background:. Crouzon syndrome (CS) is a rare form of craniosynostosis characterized by bicoronal craniosynostosis and facial features including severe midface hypoplasia, exophthalmos, and hypertelorism.
Justin Hart, DO, Stephen Lu, MD, Konstantinos Gasteratos, MD, Kongkrit Chaiyasate, MD, FACS   +3 more
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, Aaditi N Kadam, Freny R Karjodkar, Kaustubh P Sansare   +3 more
doaj   +1 more source

Midface advancement in an adult patient with Crouzon syndrome: Modified LeFort III + LeFort I osteotomy accompanied by genioplasty and nasal dorsum augmentation

Dental Research Journal, 2022
Crouzon syndrome is an autosomal dominant trait, leading to midface deficiency, undeveloped orbits, short nasal dorsum, and exophthalmos as the typical clinical features.
Milad Etemadi Sh, Golnaz Tajmiri
doaj   +1 more source

Combined soft and skeletal tissue modelling of normal and dysmorphic midface postnatal development [PDF]

, 2016
BACKGROUND: Midface hypoplasia as exemplified by Treacher Collins Syndrome (TCS) can impair appearance and function. Reconstruction involves multiple invasive surgeries with variable long-term outcomes.
Bulstrode, NW, Dunaway, D, Ferretti, P, Suttie, M, Ibrahim, A, Hammond, P, Britto, JA   +6 more
core   +1 more source

DS_10.1177_0022034519893656 – Supplemental material for PIN1 Attenuation Improves Midface Hypoplasia in a Mouse Model of Apert Syndrome

, 2019
Supplemental material, DS_10.1177_0022034519893656 for PIN1 Attenuation Improves Midface Hypoplasia in a Mouse Model of Apert Syndrome by B. Kim, H. Shin, W. Kim, H. Kim, Y. Cho, H. Yoon, J. Baek, K. Woo, Y. Lee and H.
H. Shin (8179932), K. Woo (8179941), Y. Lee (1439653), J. Baek (8179938), W. Kim (7627613), Y. Cho (3828718), B. Kim (3961577), H. Ryoo (8179944), H. Yoon (8179935), H. Kim (1486366)   +9 more
core   +1 more source

Dental and craniofacial anomalies associated with Axenfeld–Rieger syndrome

Saudi Journal of Oral Sciences, 2019
Axenfeld–Rieger syndrome (ARS) is a rare, autosomal dominant disorder with genetic and morphologic variability and characterized by ocular and nonocular clinical findings.
Amit Khatri, Prerna Beniwal, Namita Kalra, Rishi Tyagi   +3 more
doaj   +1 more source

Cleft Palate Repair: A History of Techniques and Variations

Plastic and Reconstructive Surgery, Global Open, 2022
Summary:. Orofacial clefting is a common reconstructive surgical condition that often involves the palate. Cleft palate repair has evolved over three centuries from merely achieving anatomical closure to prioritizing speech development and avoiding ...
Priyanka Naidu, MBChB, MSc, Caroline A. Yao, MD, MSc, FACS, David K. Chong, MBBS, FRACS, William P. Magee, III, MD, DDS, FACS   +3 more
doaj   +1 more source

Apert syndrome: a case report

National Journal of Clinical Anatomy, 2015
Apert syndrome was described as a triad of craniosynostosis, syndactyly and maxillary hypoplasia. The incidence of Apert syndrome is approximately one in 50,000 births.
A Barman, B C Dutta, J K Sarkar
doaj   +1 more source

Secretopathies emerge as a new class of neurocristopathies

Developmental Dynamics, EarlyView.
Abstract Neural crest cells are a transient embryonic population of cells that give rise to a wide range of structures, including craniofacial cartilage and bone, peripheral neurons and glia, as well as components of the cardiac outflow tract, among others.
Amanda Teixeira, Cassandra Millet‐Boureima, Joshua A. Moore, Loydie A. Jerome‐Majewska   +3 more
wiley   +1 more source