Results 101 to 110 of about 6,402 (203)

Obstructive sleep apnea in children [PDF]

, 2010
Childhood obstructive sleep apnea syndrome (OSAS) is characterized by recurrent episodes of partial or complete upper airway obstruction during sleep.
Fagondes, Simone Chaves, Moreira, Gustavo Antonio   +1 more
core   +3 more sources

Syndrome of the Month: Bosma Arhinia Microphthalmia Syndrome

American Journal of Medical Genetics Part A, Volume 197, Issue 11, November 2025.
Katherine J. K. Patterson, John M. Graham Jr, Natalie D. Shaw   +2 more
wiley   +1 more source

Evolution of a child with Treacher Collins syndrome undergoing physiotherapeutic treatment

Fisioterapia em Movimento
Introduction Treacher Collins syndrome, or mandibulofacial dysostosis, is a hereditary disorder and is manifested by craniofacial malformations. The incidence is close to one case per 40,000 live births, without relation to gender or race.
Bárbara Gabriela da S. Rodrigues, Juliane Leonardo Oliveira Silva, Pryscilla Gualberto Guimarães, Cibelle Kayenne Martins Roberto Formiga, Fabiana Pavan Viana   +4 more
doaj   +1 more source

Berry syndrome: A case report and review of literature

Journal of Indian Academy of Oral Medicine and Radiology, 2017
Berry syndrome or Treacher Collins syndrome (TCS) is an autosomal dominant disorder of craniofacial development with variable expressivity. The most common manifestations of TCS are the antimongoloid slanting of the palpebral fissures, colobomas of the ...
Mayuri P Suryavanshi, Sonia J Sodhi, Lata M Kale, Swati J Rathod, Vishwas D Kadam   +4 more
doaj   +1 more source

Corneal Dermoid [PDF]

, 2011
A 20 years old boy presented with left corneal mass. The mass involved entire cornea extending to the sclera. The mass had a skin like surface and protruded outside the palpebral aperture.
Achar, A, Hegde, S, Kadri, R, Kudva, AA
core  

Misdiagnosis of Tracher-Collins Syndrome Initially Attributed to Drug Teratogenicity: A Moroccan Case Report

Balkan Journal of Medical Genetics
Treacher Collins syndrome (TCS) is a rare congenital disorder of craniofacial development characterized by numerous developmental anomalies that are restricted to the head and neck. Most TCS cases are inherited in an autosomal dominant manner.
Lamzouri A, EL Rherbi A, Ratbi I, Laarabi FZ, Chahboune R, Elalaoui SC, Hamdaoui H, Bencheikh RS, Sefiani A   +8 more
doaj   +1 more source

Complete Agenesis of Right Half of Soft Palate—A Case Report

Indian Journal of Plastic Surgery
Agenesis of soft palate is an extremely rare occurrence and is usually seen in conjunction with other congenital anomalies like Nager syndrome, Treacher Collins syndrome, and multiple congenital anomalies.
Ishan Agnihotri, Bibhuti Bhusan Nayak
doaj   +1 more source

Interim obturator in an infant with Treacher Collins syndrome: Review and chairside modification in impression making

Contemporary Clinical Dentistry, 2011
Treacher Collins syndrome has been described as a syndrome involving 1st and 2nd branchial arches, affecting various organs in the craniofacial region.
Sudhir Bhandari, Meena Aras, Sonika Bakshi   +2 more
doaj   +1 more source

Treacher Collins Syndrome: A Case Report and Review

GAIMS Journal of Medical Sciences
Treacher Collins syndrome is an autosomal dominant genetic disorder that results from improper development of the first and second pharyngeal arches. Disruption in the formation and migration of neural crest cells leads to facial malformation. Face shows
Sagnik Roy, Nivedita Roy
doaj   +1 more source

Mild Form of Treacher Collins Syndrome Imitating Juvenile Otosclerosis

Case Reports in Pediatrics, 2012
Treacher Collins syndrome (TCS) is an inherited developmental disorder. More than 40% of individuals with TCS have conductive hearing loss attributed to external and middle ear anomalies.
Karol Zeleník, Pavel Komínek
doaj   +1 more source