Search results for "cleft lip"

showing 10 items of 32 documents

Congenital lower lip pits : Van der Woude syndrome

2018

The Van der Woude syndrome is a rare autosomal dominant development malformation characterized by a paramedian lip pits and /or sinuses or conical elevation of lower lip associated with cleft lip and or palate. These congenital lip pits usually appear clinically in the vermilion border of lip, with or without secretion. The critical region of VWS has been identified to be at Iq32 to 41 with high, but incomplete penetrance and variable expressivity. Therapeutic intervention is generally required for cosmetic reason or when recurrent inflammation is present. Dental surgeon should be aware of this syndrome, as it is associated with variety of other congenital malformation. van der woude syndro…

Oral Medicine and Pathologybusiness.industryLower lipRecurrent inflammationCase ReportAnatomymedicine.disease:CIENCIAS MÉDICAS [UNESCO]Penetrance03 medical and health sciencesstomatognathic diseases0302 clinical medicinemedicine.anatomical_structurestomatognathic systemBilateral cleft lip030225 pediatricsUNESCO::CIENCIAS MÉDICASmedicineVan der Woude syndrome030212 general & internal medicineVermilion borderbusinessGeneral DentistryCongenital lower lip pits
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Orofacial features and medical profile of eight individuals with Kabuki syndrome

2019

Background To evaluate oral, craniofacial and systemic characteristics of eight patients with Kabuki syndrome (KS), aged between 3 and 16 years old. Material and Methods In this retrospective study, medical records of all patients were reviewed for information on family history, growth and development, medications in use, general systemic complications and oral and craniofacial characteristics. Results The medical alterations found included recurrent infections such as pneumonia and otitis media (n = 6), cardiovascular malformations (n = 4), kidney abnormalities (n = 2), epilepsy (n = 2) and visual deficiency (n = 2). The individuals exhibited dental caries (n = 5), agenesis (n = 5), delaye…

Pediatricsmedicine.medical_specialtyAdolescentCleft LipDental CariesAnodontia03 medical and health sciences0302 clinical medicinemedicineMicrodontiaHumansAbnormalities MultipleCraniofacialFamily historyChildGeneral DentistryAnodontiaRetrospective StudiesTooth Abnormalitiesbusiness.industryResearch030206 dentistryEnamel hypoplasia:CIENCIAS MÉDICAS [UNESCO]Medically compromised patients in Dentistrymedicine.diseaseHematologic DiseasesCleft Palatestomatognathic diseasesOtitisVestibular DiseasesOtorhinolaryngologyChild PreschoolFaceAgenesisUNESCO::CIENCIAS MÉDICASSurgerymedicine.symptombusinessKabuki syndromeMedicina Oral Patología Oral y Cirugia Bucal
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Predictive validity of the GOSLON Yardstick index in patients with unilateral cleft lip and palate: A systematic review

2017

Among the various indices developed for measuring the results of treatment in patients born with unilateral cleft lip and palate (UCLP), the GOSLON Yardstick index is the most widely used to assess the efficacy of treatment and treatment outcomes, which in UCLP cases are closely linked to jaw growth. The aim of this study was to conduct a systematic review to validate the predictability of growth using the GOSLON Yardstick in patients born with UCLP. A systematic literature review was conducted in four Internet databases: Medline, Cochrane Library, Scopus and Embase, complemented by a manual search and a further search in the databases of the leading journals that focus on this topic. An el…

Predictive validityIndex (economics)Systematic ReviewsCleft LipOral MedicineMEDLINEScopusCleft Lip and Palatelcsh:MedicineDentistrySurgical and Invasive Medical ProceduresOrthodonticsCochrane LibraryResearch and Analysis MethodsDatabase and Informatics Methods03 medical and health sciences0302 clinical medicineMedicine and Health SciencesCongenital DisordersMorphogenesisHumansMedicineIn patientBirth DefectsLongitudinal Studies030212 general & internal medicineDatabase Searchinglcsh:ScienceMultidisciplinarybusiness.industrylcsh:RBiology and Life SciencesGoslon yardstick030206 dentistryResearch AssessmentCleft PalateSystematic reviewOtorhinolaryngologyResearch Designlcsh:QbusinessResearch ArticleDevelopmental BiologyPLOS ONE
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Presurgical Preparation of Infants With Unilateral Cleft Lip and Palate: The SAC-PP-MR Innovative Technique

2018

In this article, we demonstrate an effective, cheap, and fast way to shape the nasal alar cartilage in patients with unilateral cleft lip and palate. This technique straightens the vomer and brings the philtrum, columella, premaxilla, and the maxillary frenum to the midsagittal plane, while the alveolar ridges are shaped and positioned. This reduces the lip and palatal cleft to zero even in a 4-week period.

PremaxillaCleft LipAlar cartilageVomer03 medical and health sciences0302 clinical medicinePreoperative CareAlveolar ProcessHumansMedicineIn patientPresurgical orthopedics030223 otorhinolaryngologyOrthodonticsColumellaPhiltrumbusiness.industryInfant030206 dentistryLipSagittal planeCleft Palatemedicine.anatomical_structureOtorhinolaryngologyOral SurgerybusinessThe Cleft Palate-Craniofacial Journal
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Contribution of polymorphisms in genes associated with craniofacial development to the risk of nonsyndromic cleft lip and/or palate in the Brazilian …

2012

Background and Objective: Nonsyndromic cleft lip and/or palate (NSCL/P) is a complex disease associated with both genetic and environmental factors. One strategy for identifying of possible NSCL/P genetic causes is to evaluate polymorphic variants in genes involved in the craniofacial development. Design: We carried out a case-control analysis of 13 single nucleotide polymorphisms in 9 genes related to craniofacial development, including TBX1, PVRL1, MID1, RUNX2, TP63, TGFB3, MSX1, MYH9 and JAG2 , in 367 patients with NSCL/P and 413 unaffected controls from Brazil to determine their association with NSCL/P. Results: Four out of 13 polymorphisms (rs28649236 and rs4819522 of TBX1, rs7940667 o…

RiskGenotypeCleft LipPopulationSingle-nucleotide polymorphismOdontologíaGrowthBiologystomatognathic systemTP63GenotypeHumansCraniofacialAlleleeducationMaxillofacial DevelopmentGeneral DentistryGeneticseducation.field_of_studyPolymorphism GeneticOral Medicine and PathologySkullCase-control study:CIENCIAS MÉDICAS [UNESCO]Ciencias de la saludGenotype frequencyCleft PalateOtorhinolaryngologyCase-Control StudiesUNESCO::CIENCIAS MÉDICASSurgeryResearch-ArticleBrazil
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Influence of patient-related factors on intraoperative blood loss during double opposing Z-plasty Furlow palatoplasty and buccal fat pad coverage:A p…

2022

Background: Surgical procedures including palatoplasty have a risk for complications. The aim of this study was to investigate the intraoperative and early postoperative blood loss using the buccal fat pad (BFP) during cleft lip and/or cleft palate (CL/P) surgery. Material and Methods: This prospective study included a total of 109 patients with cleft palate (CP) during a three-month period of treatment at Hasanuddin University Dental Hospital (permanent center) and charity trips in rural parts of Eastern Indonesia. All patients were treated with DOZ Furlow technique combined with BFP graft. Before and after surgery, the total amount of intraoperative blood loss was calculated by measuring …

cleft palateBuccal fat padSDG 3 - Good Health and Well-being/dk/atira/pure/sustainabledevelopmentgoals/good_health_and_well_beingcomplicationcleft lippalatoplastyGeneral DentistryUNESCO:CIENCIAS MÉDICAS
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Neurophysiological changes and chronic pain in cleft patients

2019

Abstract The aim of this study was to evaluate if patients after orofacial cleft repair experience neurophysiological changes with consecutive chronic pain states after surgery. Patients (n = 48) with a repaired orofacial cleft (CLP) recruited in a support group took part in a survey including five questionnaires. They revealed pain states, described cleft situation and history, and epidemiological data. Patients' quality of life and psychological comorbidity after the surgical procedures were assessed with the Oral Health Impact Profile (OHIP), the Giessen Subjective Complaints List (GSCL) and the Hospital Anxiety and Depression Scale (HADS). Furthermore, psychosocial impairment was docume…

medicine.medical_specialtyCleft LipPsychological interventionAnxietyHospital Anxiety and Depression Scale03 medical and health sciences0302 clinical medicineQuality of lifeSurveys and QuestionnairesmedicineHumansChildDepression (differential diagnoses)Depressionbusiness.industryChronic pain030206 dentistrymedicine.diseaseComorbidityOtorhinolaryngologyChild Preschool030220 oncology & carcinogenesisQuality of LifePhysical therapyAnxietySurgeryChronic PainOral Surgerymedicine.symptombusinessPsychosocialJournal of Cranio-Maxillofacial Surgery
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Novel missense mutation of the TP63 gene in a newborn with Hay-Wells/Ankyloblepharon-Ectodermal defects-Cleft lip/palate (AEC) syndrome: clinical rep…

2021

Abstract Introduction Ankyloblepharon-ectodermal defects-cleft lip/palate (AEC) syndrome, also known as Hay-Wells syndrome, is a rare genetic syndrome with ectodermal dysplasia. About 100 patients have been reported to date. It is associated to a heterozygous mutation of the tumor protein p63 (TP63) gene, located on chromosome 3q28. Typical clinical manifestations include: filiform ankyloblepharon adnatum (congenital adherence of the eyelids), ectodermal abnormalities (sparse and frizzy hair, skin defects, nail alterations, dental changes and hypohidrosis), and cleft lip/palate. Diagnostic suspicion is based on clinical signs and confirmed by genetic testing. Patient’s presentation We hereb…

medicine.medical_specialtyEctodermal dysplasiaHay–Wells syndromeCleft LipAnkyloblepharonMutation MissenseErythrodermaCase ReportEctodermal dysplasiaPediatricsRJ1-570TP63medicineMissense mutationHumansEye Abnormalitiesbusiness.industryTumor Suppressor ProteinsAEC syndromeInfant NewbornTumor protein p63 geneEyelidsmedicine.diseaseAnkyloblepharon-ectodermal defects-cleft lip/palate syndromeDermatologyCleft Palatemedicine.anatomical_structureHay-Wells syndromeScalpAgenesisFemaleAEC syndrome Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome Congenital skin disorders Ectodermal dysplasia Hay-Wells syndrome Tumor protein p63 genebusinessTranscription FactorsCongenital skin disordersItalian journal of pediatrics
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NAM Therapy-Evidence-Based Results

2020

Many orthodontists working on patients with cleft lip and palate (CLP) have shown great enthusiasm for presurgical infant orthopedics (PSIO) to improve surgical outcomes with minimal intervention. Even though every clinician aims to use the best treatment modality for their patients, PSIO effects can be confounded by surgical type and timing of the primary repair, as is discussed in many studies. In such cases, one should be cautious when evaluating the particular outcomes for patients with CLP since it is difficult to differentiate the sole effect of an individual surgical or orthodontic intervention. As with any treatment methodology, nasoalveolar molding (NAM) has both benefits and limi…

medicine.medical_specialtyEvidence-based practiceinfant orthopedicmedicine.medical_treatmentCleft Lipmidfacial growthNoseBurden of care03 medical and health sciencesPrimary repair0302 clinical medicineIntervention (counseling)medicineDeformityMaxillaHumansOrthopedic Procedures030223 otorhinolaryngologyIntensive care medicineMaxillary growthReduction (orthopedic surgery)business.industryInfant orthopedicsInfant030206 dentistryPlastic Surgery ProceduresCleft PalateOtorhinolaryngologyfacial growthOral Surgerymedicine.symptombusinessnonsyndromic clefting
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Two-Stage operation for cleft palate

1963

medicine.medical_specialtyTwo stage operationbusiness.industryCleft LipSurgery.plasticSurgeryCleft PalateOtorhinolaryngologymedicineHumansSurgerySurgery PlasticbusinessPlasticsBritish Journal of Plastic Surgery
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