Results 11 to 20 of about 241,816 (288)
Mandibular growth in infants with Robin sequence treated with the Tübingen palatal plate
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 +7 more
doaj +1 more source
Pleomorphic adenoma of the palate - A case series
Rationale and Patient Concerns: This article highlights the case report of pleomorphic adenoma (PA) of the palate in a 37-year-old female patient and a 34-year-old male patient.
S Parvathi +2 more
doaj +1 more source
Detection of Single Nucleotide Polymorphism Rs2013162 of IRF6 Gene in Patient with Cleft Lip and Palate [PDF]
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) +1 more
core +2 more sources
Interaction between IRF6 and TGFA Genes Contribute to the Risk of Nonsyndromic Cleft Lip/Palate [PDF]
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 +18 more
core +10 more sources
Aims: The aims of the study are to describe the epidemiological characteristics of the patients with cleft lip and palate (CLP) treated at Specialized National Hospital in Venezuela.
Katherine Moleiro +6 more
doaj +1 more source
Incidence of cleft lip and palate in Gorgan - Northern Iran: An epidemiological study [PDF]
Objective: Cleft lip with or without cleft palate is the most common orofacial congenital anomaly among live births. This study was carried out to determine the incidence rate of oral clefting in Gorgan, Northern Iran during 2004-2009.
Golalipour, M.J. +3 more
core +2 more sources
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 +3 more
doaj +1 more source
Bi-allelic GAD1 variants cause a neonatal onset syndromic developmental and epileptic encephalopathy. [PDF]
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 +30 more
core +2 more sources
The objective of this retrospective pilot study was to describe potential risk factors for failure of hard palate mucoperiosteal flaps (HPF) transposed for closure of oronasal communication. Dogs (n = 28) with acquired oronasal communication defects were
Kendall Taney +3 more
doaj +1 more source
Focal Unilateral Palatal Myoclonus Causing Objective Clicking Tinnitus without Uvula Elevation Diagnosed by Concurrent Auscultation [PDF]
Palatal myoclonus generally entails a visible elevation of the palate and uvula and may be accompanied by myoclonus of other oropharyngeal muscles. A 55-year-old man presented with left ear clicking and hyperacusis.
Chindhuri Selvadurai +1 more
doaj +1 more source

