Results 101 to 110 of about 6,877 (203)
Flexibility within the middle ears of vertebrates [PDF]
Introduction and aims: Tympanic middle ears have evolved multiple times independently among vertebrates, and share common features. We review flexibility within tympanic middle ears and consider its physiological and clinical implications.
Baird +36 more
core +1 more source
Exon-phase symmetry and intrinsic structural disorder promote modular evolution in the human genome [PDF]
A key signature of module exchange in the genome is phase symmetry of exons, suggestive of exon shuffling events that occurred without disrupting translation reading frame.
Adams +62 more
core +1 more source
Treacher-Collins syndrome (TCS) is a rare congenital disease known to be associated with a difficult airway and is challenging for anesthesiologists practicing pediatric anesthesia.
Babak Eslami +5 more
doaj +1 more source
Treacher-Collins syndrome [PDF]
INTRODUCTION- Treacher Collins syndrome (TCS) is a rare syndrome inherited as autosomal dominant. The affected children may vary in severity ranging from minimal features as slanting of palpebral fissures to major features of craniofacial ...
Kumar , PD, Kumari , CK, Sarella, LK
core +1 more source
Evolution of a child with Treacher Collins syndrome undergoing physiotherapeutic treatment
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 +4 more
doaj +1 more source
Berry syndrome: A case report and review of literature
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 +4 more
doaj +1 more source
We present a rare case of Trecher Collins Syndrome.DOI: http://dx.doi.org/10.3126/jnps.v33i3.7896 J. Nepal Paediatr. Soc.
Abhijeet Saha +2 more
openaire +2 more sources
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 +8 more
doaj +1 more source
Treacher Collins Syndrome: A Case Report and Review
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
Complete Agenesis of Right Half of Soft Palate—A Case Report
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

