Results 21 to 30 of about 235,287 (271)

Detection of Single Nucleotide Polymorphism Rs2013162 of IRF6 Gene in Patient with Cleft Lip and Palate [PDF]

, 2019
Background: Cleft lip and palate are congenital disorders which induce affected individuals medically, socially and psychologically. The objective of this study was to investigate the association of Single Nucleotide Polymorphism(SNP); rs2013162 of ...
Shehzad, H. (Husnain), Shehzad, O. (Osheen)   +1 more
core   +3 more sources

Mandibular growth in infants with Robin sequence treated with the Tübingen palatal plate

Head & Face Medicine, 2019
Background Robin sequence (RS) is characterized by mandibular retrognathia, glossoptosis and upper airway obstruction. Whether mandibular catch-up growth may occur in RS is yet controversial.
Cornelia Wiechers, Wolfgang Buchenau, Jörg Arand, Anne-Friederike Oertel, Katharina Peters, Silvia Müller-Hagedorn, Bernd Koos, Christian F. Poets   +7 more
doaj   +1 more source

Transcriptomic analysis of the upper lip and primary palate development in mice

Frontiers in Genetics, 2023
Background: Normal fusion of the upper lip and primary palate is a complex process involving a series of characteristic and orderly regulated cellular events.
Sini Cai, Nuo Si, Yanyang Wang, Ningbei Yin   +3 more
doaj   +1 more source

Interaction between IRF6 and TGFA Genes Contribute to the Risk of Nonsyndromic Cleft Lip/Palate [PDF]

, 2012
Previous evidence from tooth agenesis studies suggested IRF6 and TGFA interact. Since tooth agenesis is commonly found in individuals with cleft lip/palate (CL/P), we used four large cohorts to evaluate if IRF6 and TGFA interaction contributes to CL/P ...
Alexandre R. Vieira, Andrew C. Lidral, Ariadne Letra, Baiba Lace, Brian C. Schutte, Dale J. Hedges, Eduardo E. Castilla, Ieda M. Orioli, Inga Kempa, Jeffrey C. Murray, Joanne L. Prasad, Jose M. Granjeiro, Lina Moreno, Mary L. Marazita, Renata F. Fonseca, Renato Menezes, Sandra Daack-Hirsch, Toby G. McHenry, Walid Fakhouri   +18 more
core   +10 more sources

The Use of Eye-tracking Technology in Cleft Lip: A Literature Review

Plastic and Reconstructive Surgery, Global Open, 2023
Background:. Eye-tracking has become an increasingly popular research tool within the field of cleft lip and/or palate (CL+/−P). Despite this, there are no standardized protocols for conducting research.
Alexander T. Plonkowski, R. William F. Breakey, MRCS, PhD, BSc, Jenny C. A. Read, BA, MSc, DPhil, David C. G. Sainsbury, MBBS, MSc, FRCS(Plast)   +3 more
doaj   +1 more source

Impact of early synchronous lip and palatal repair on speech [PDF]

, 2013
<b><i>Aims:</i></b> The purpose of this study was to describe articulation and resonance characteristics of Ugandan English-speaking children with cleft lip and palate (CLP) after synchronous lip and palatal closure (Sommerlad ...
Bettens, Kim, D'haeseleer, Evelien, De Ley, Sophia, Galiwango, George, Hodges, Andrew, Luyten, Anke, Van Lierde, Kristiane, Vermeersch, Hubert   +7 more
core   +1 more source

Monogenic Versus Multifactorial Inheritance in the Development of Isolated Cleft Palate: A Whole Genome Sequencing Study

Frontiers in Genetics, 2022
Craniofacial morphogenesis is highly complex, as is the anatomical region involved. Errors during this process, resulting in orofacial clefts, occur in more than 400 genetic syndromes.
Baiba Lace, Sander Pajusalu, Sander Pajusalu, Sander Pajusalu, Diana Livcane, Ieva Grinfelde, Ieva Grinfelde, Ilze Akota, Ieva Mauliņa, Biruta Barkāne, Janis Stavusis, Inna Inashkina   +11 more
doaj   +1 more source

Racial Disparities in Cleft Palate Repair.

Plastic and Reconstructive Surgery, 2019
BACKGROUND Various factors can influence outcomes in cleft palate care. This study sought to determine the impact of race on admissions, hospital costs, and short-term complications in cleft palate repair.
R. Wu, C. Peck, Blake N. Shultz, R. Travieso, D. Steinbacher   +4 more
semanticscholar   +1 more source

A case report of acampomelic campomelic dysplasia and operative difficulties in cleft palate reconstruction

Indian Journal of Plastic Surgery, 2016
Acampomelic campomelic dysplasia (CD) is a type of CD (CD; OMIM #114290), a rare form of congenital short-limbed dwarfism and is due to mutations in SOX9 gene family.
M. Pasupathy, Vasant Radhakrishnan, Hirji Sorab Adenwalla, Puthucode V. Narayanan   +3 more
doaj   +1 more source

Study protocol for a multicenter, multinational, observational registry of epidemiology, treatment and outcome of patients with Robin sequence

Head & Face Medicine, 2023
Background Robin sequence (RS) is a congenital condition characterized by micrognathia, glossoptosis and upper airway obstruction. Diagnosis and treatment are characterized by heterogeneity, resulting in a lack of uniformly collected data.
Anna-Lisa Oechsle, Cornelia Wiechers, Veronique Abadie, Francois Abel, Corstiaan Breugem, Christian F. Poets   +5 more
doaj   +1 more source