Results 21 to 30 of about 247,308 (380)

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

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

Dental Implant Treatment for a Patient with Bilateral Cleft Lip and Palate [PDF]

, 2008
Dental reconstruction in the cleft space is difficult in some patients with cleft lip and palate because of oronasal fistulas. Most of these patients receive a particle cancellous bone marrow (PCBM) graft to close the alveolar cleft, and secondary bone ...
Honda, Kozo, Kagawa, Toshimasa, Kanou, Miwa, Kuboki, Takuo, Sawaki, Masako, Shirasu, Nobuaki, Sugahara, Toshio, Ueno, Takaaki   +7 more
core   +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

Pbx loss in cranial neural crest, unlike in epithelium, results in cleft palate only and a broader midface. [PDF]

, 2018
Orofacial clefting represents the most common craniofacial birth defect. Cleft lip with or without cleft palate (CL/P) is genetically distinct from cleft palate only (CPO).
Berkes, Blaschke, Brendolan, Britanova, Buck, Bush, Capellini, Capellini, Capellini, Capellini, Choe, Clement-Jones, Cox, Cuadra-Blanco, Dixon, Dobreva, Elahi, Ferguson, Ferguson, Ferretti, Ficara, Ficara, Fuchs, Golonzhka, Gordon, Gordon, Gosain, Grebbin, Gritli-Linde, Gritli-Linde, Hebert, Hessle, Hill, Hilliard, Ho, Howe, Hurtado, Kim, Kim, Koss, Kousa, Lan, Lane, Leslie, Lewis, Li, Lidral, Longobardi, Losa, Manyama, Marazita, Martik, McCulley, Miletich, Minoux, Moens, Murphy, Okano, Pauws, Percival, Rhee, Richman, Roberts, Rosset, Sagerstrom, Satokata, Schnabel, Selleri, Selleri, Stankunas, Sun, Tam, Villaescusa, Welsh, Young, Yu, Yu, Zeytinoglu, Zhang   +78 more
core   +1 more source

Bi-allelic GAD1 variants cause a neonatal onset syndromic developmental and epileptic encephalopathy. [PDF]

, 2020
Developmental and epileptic encephalopathies are a heterogeneous group of early-onset epilepsy syndromes dramatically impairing neurodevelopment. Modern genomic technologies have revealed a number of monogenic origins and opened the door to therapeutic ...
Alix, E, Alkaya, DU, Ashrafzadeh, F, Becker, F, Bilguvar, K, Chatron, N, de Bellescize, J, EuroEpinomics-RES consortium AR working group, Gunes, N, Hardies, K, Hussien, H, Karimiani, EG, Kok, F, Labalme, A, Lerche, H, Lesca, G, Maroofian, R, May, P, Morsy, H, Moslemi, A-R, Nabil, A, Najafi, M, Omar, T, Poulat, A-L, Ramos, L, Roselli, S, Sanlaville, D, Schmidts, M, Tajsharghi, H, Tuysuz, B, Weckhuysen, S   +30 more
core   +2 more sources

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

Timing Of Primary Surgery for cleft palate (TOPS): protocol for a randomised trial of palate surgery at 6 months versus 12 months of age

BMJ Open, 2019
Introduction Cleft palate is among the most common birth abnormalities. The success of primary surgery in the early months of life is crucial for successful feeding, speech, hearing, dental development and facial growth.
William Shaw, G. Semb, A. Lohmander, C. Persson, E. Willadsen, J. Clayton-Smith, I. K. Trindade, K. Munro, C. Gamble, N. Harman, Elizabeth Conroy, D. Weichart, P. Williamson   +12 more
semanticscholar   +1 more source

Three-dimensional reconstruction of systematic histological sections: application to observations on palatal shelf elevation

International Journal of Oral Science, 2021
Normal mammalian secondary palate development undergoes a series of processes, including palatal shelf (PS) growth, elevation, adhesion and fusion, and palatal bone formation. It has been estimated that more than 90% of isolated cleft palate is caused by
Weilong Liu, Xiaoming Wang, Yinuo Wang, Yahong Wang, Jing Zhang, Bing Shi, Chenghao Li   +6 more
doaj   +1 more source

Targeted Re-Sequencing of the 2p21 Locus Identifies Non-Syndromic Cleft Lip Only Novel Susceptibility Gene ZFP36L2

Frontiers in Genetics, 2022
rs7590268 present on the 2p21 locus was identified to be associated with non-syndromic cleft lip with or without cleft palate (NSCL/P) in several populations, including the Chinese Han population, indicating that 2p21 was a susceptibility locus for NSCL ...
Mu-Jia Li, Jia-Yu Shi, Qiu-Shuang Zhu, Bing Shi, Zhong-Lin Jia   +4 more
doaj   +1 more source