Search results for "Craniosynostosis"

showing 10 items of 13 documents

Apert Syndrome With FGFR2 758 C > G Mutation: A Chinese Case Report

2018

Background: Apert syndrome is considered as one of the most common craniosynostosis syndromes with a prevalence of 1 in 65,000 individuals, and has a close relationship with point mutations in FGFR2 gene.Case report: Here, we described a Apert syndrome case, who was referred to genetic consultation in our hospital with the symptom of craniosynostosis and syndactyly of the hands and feet. Craniosynostosis, midfacial retrusion, steep wide forehead, larger head circumference, marked depression of the nasal bridge, short and wide nose and proptosis could be found obviously, apart from these, ears were mildly low compared with normal children and there was no cleft lip and palate. Mutation was i…

0301 basic medicinemusculoskeletal diseasesPediatricsmedicine.medical_specialtycongenital hereditary and neonatal diseases and abnormalitiesNasal bridgelcsh:QH426-470Case ReportApert syndromeCraniosynostosis03 medical and health sciencesExonsymbols.namesake0302 clinical medicineGeneticsmedicineSyndactylyGenetics (clinical)NoseSanger sequencingbusiness.industryPoint mutationmedicine.diseaseexons sequencingcraniosynostosislcsh:Genetics030104 developmental biologymedicine.anatomical_structureFGFR2genetic mutationsymbolsMolecular Medicinebusiness030217 neurology & neurosurgeryApert syndromeFrontiers in Genetics
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Kosaki overgrowth syndrome: A novel pathogenic variant in PDGFRB and expansion of the phenotype including cerebrovascular complications

2020

Heterozygous activating variants in platelet-derived growth factor, beta (PDGFRB) are associated with phenotypes including Kosaki overgrowth syndrome (KOGS), Penttinen syndrome and infantile myofibromatosis (IM). Here, we present three new cases of KOGS, including a patient with a novel de novo variant c.1477A > T p.(Ser493Cys), and the oldest known individual age 53 years. The KOGS phenotype includes characteristic facial features, tall stature, scoliosis, hyperelastic thin skin, lipodystrophy, variable intellectual and neurological deterioration, and abnormalities on brain imaging. Long-term outcome is unknown. Our cases confirm the phenotypic spectrum includes progressive flexion contrac…

AdultMale0301 basic medicinePathologymedicine.medical_specialtyInfantile myofibromatosisPDGFRBScoliosis030105 genetics & heredityCraniosynostosisReceptor Platelet-Derived Growth Factor beta03 medical and health sciencesCamptodactylyGeneticsmedicineHumansJoint dislocationStrokeGrowth DisordersGenetics (clinical)business.industryGenetic VariationMiddle Agedmedicine.diseaseCerebrovascular DisordersPhenotype030104 developmental biologymedicine.symptomLipodystrophybusinessClinical Genetics
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Bone Fusion in Normal and Pathological Development is Constrained by the Network Architecture of the Human Skull

2016

The premature fusion of cranial bones, craniosynostosis, affects the correct development of the skull producing morphological malformations in newborns. To assess the susceptibility of each craniofacial articulation to close prematurely, we used a network model of the skull to quantify the link reliability (an index based on stochastic block modeling and Bayesian inference) of each articulation. We show that, of the 93 human skull articulations at birth, the few articulations that are associated with nonsyndromic craniosynostosis conditions have statistically significant lower reliability scores than the others. In a similar way, articulations that close during the normal postnatal developm…

Craniometria0301 basic medicineSciencemedicine.medical_treatmentBiologyCraniosynostosesQuantitative Biology - Quantitative MethodsBone and BonesArticleCraniosynostosisXarxes (Matemàtica)Craniosynostoses03 medical and health sciencesHuman skullChemical engineeringCraniosynostosismedicineHumansCraniofacialTissues and Organs (q-bio.TO)PathologicalQuantitative Methods (q-bio.QM)Bone DevelopmentMultidisciplinarySkullQInfant NewbornRIngeniería químicaBayes TheoremQuantitative Biology - Tissues and OrgansAnatomymedicine.diseaseSkullSpinal Fusion030104 developmental biologymedicine.anatomical_structureFOS: Biological sciencesSpinal fusion2045-2322Crani--Malformacions--TractamentMedicineNeural Networks ComputerArticulation (phonetics)Enginyeria químicaAlgorithmsScientific Reports
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Cranial deformations in an Iron Age population from Münsingen-Rain, Switzerland

2008

The aim of this paper is an examination of cranial fluctuating asymmetry (FA) and deformations in the prehistoric population of Munsingen-Rain (La Tene period, Switzerland). The material consists of 76 skulls. Three cases of craniosynostosis, one scaphocephalic skull with complete obliteration of the sagittal suture and two plagiocephalic skulls were identified. CT scans showed that premature closure of the frontosphenoidal suture caused these plagiocephalies. For three asymmetrically deformed skulls, differential diagnosis indicates torticollis (wry neck). Another four skulls exhibit strongly developed asymmetries of the cranium and mandible, but an aetiological diagnosis was not possible.…

Fibrous jointArcheologyeducation.field_of_studyPopulationMandibleAnatomyBiologymedicine.diseaseCraniosynostosisSagittal sutureSkullmedicine.anatomical_structureAnthropologymedicineeducationPaleopathologyTorticollisInternational Journal of Osteoarchaeology
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Phenotypic expression of the fibroblast growth factor receptor 3 (FGFR3) mutation P250R in a large craniosynostosis family.

1997

The craniosynostosis syndromes are a heterogeneous group of sporadic, autosomal dominant disorders with significant clinical overlap. Recently, we described a large family with autosomal dominant craniosynostosis suggestive of Saethre-Chotzen syndrome, in which linkage to the Saethre-Chotzen syndrome loci on 7p had been excluded. We now report the presence of a mutation in the fibroblast growth factor receptor 3 (FGFR3) in this family. The mutation, P250R, had been previously reported in 10 patients with non-syndromic craniosynostosis. Variable expression of this mutation is evident especially in two additional members of this family, one of whom is severely affected with pancraniosynostosi…

MaleTurkish populationGenetic LinkageBiologyMuenke syndromeCraniosynostosisVariable ExpressionCraniosynostosesGenetic linkageGeneticsmedicineHumansReceptor Fibroblast Growth Factor Type 3Genetics (clinical)GeneticsGenetic heterogeneityInfant NewbornInfantProtein-Tyrosine KinasesFibroblast growth factor receptor 3medicine.diseaseReceptors Fibroblast Growth FactorPedigreePhenotypeMutationMutation (genetic algorithm)FemaleResearch ArticleJournal of Medical Genetics
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Boy with pseudohypoparathyroidism type 1a caused byGNASgene mutation (deltaN377), Crouzon-like craniosynostosis, and severe trauma-induced bleeding

2009

We report on a 6-month-old boy with craniosynostosis, pseudohypoparathyroidism type 1a (PHP1A), and a GNAS gene mutation. He had synostoses of the coronal, frontal, and sagittal sutures, brachyturricephaly, and hydrocephaly. He also had congenital hypothyroidism, round face, full cheeks, shortness of limbs, mild developmental delay, and muscular hypotonia. Because of progressive hydrocephaly, the synostosis was corrected surgically but circulatory decompensation led to disseminated intravascular coagulation and cerebral infarctions. Our patient died 8 days later. Postmortem molecular studies of GNAS, the gene for guanine nucleotide-binding protein, alpha-stimulating activity polypeptide (ge…

Malemedicine.medical_specialtyPathologyCraniosynostosisFatal OutcomeInternal medicineChromograninsCongenital HypothyroidismGTP-Binding Protein alpha Subunits GsGeneticsmedicineGNAS complex locusHumansGenetic Predisposition to DiseaseGenetics (clinical)PseudohypoparathyroidismDisseminated intravascular coagulationbiologyMuscular hypotoniabusiness.industryCraniofacial DysostosisInfantDysostosisSynostosismedicine.diseaseCongenital hypothyroidismEndocrinologyBrain InjuriesPseudohypoparathyroidismMutationbiology.proteinbusinessIntracranial HemorrhagesHydrocephalusAmerican Journal of Medical Genetics Part A
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Q289P mutation in the FGFR2 gene: first report in a patient with type 1 Pfeiffer syndrome.

2008

When normal development and growth of the calvarial sutures is disrupted, craniosynostosis (premature calvarial suture fusion) may result. Classical craniosynostosis syndromes are autosomal dominant traits and include Apert, Pfeiffer, Crouzon, Jackson-Weiss, and Saethre-Chotzen syndromes. In these conditions, there is premature fusion of skull bones leading to an abnormal head shape, ocular hypertelorism with proptosis, and midface hypoplasia. It is known that mutations in the fibroblast growth factor receptors 1, 2, and 3 cause craniosynostosis. We report on a child with a clinically diagnosed Pfeiffer syndrome that shows the missense point mutation Q289P in exon 8 of the FGFR2 gene. This …

Malemusculoskeletal diseasescongenital hereditary and neonatal diseases and abnormalitiesPathologymedicine.medical_specialtyCraniosynostosisSettore MED/38 - Pediatria Generale E SpecialisticaHumansPoint MutationMedicineMissense mutationReceptor Fibroblast Growth Factor Type 2HypertelorismGeneticsFibrous jointbusiness.industryFibroblast growth factor receptor 2Craniofacial DysostosisInfantDysostosisExonsAcrocephalosyndactyliamedicine.diseaseSkullPhenotypemedicine.anatomical_structurePfeiffer - Crouzon - Apert - Craniosynostosis - Finger and toes abnormalities - Fibroblast growth factor receptorPediatrics Perinatology and Child HealthPfeiffer syndromeFemalemedicine.symptombusiness
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Subjective Assessment of Head and Facial Appearance in Children with Craniosynostoses after Surgical Treatment

2018

Background: Craniosynostoses are congenital defects in the construction of the skull involving premature fusion of one or more cranial sutures. Premature fusion of sutures causes characteristic skull deformation(s). This affect the structure and thus the appearance of the entire head and face. The aim of this study was to analyze parents&rsquo

Pediatricsmedicine.medical_specialtyLeadership and ManagementHead (linguistics)craniosinostosis; results of surgery; craniofacial disfigurement; clinical survey; subjective assessment; surgical outcomeslcsh:MedicineHealth Informaticscraniofacial disfigurementCraniosynostosessurgical outcomesAffect (psychology)ArticleCraniosynostosis03 medical and health sciencesInterpersonal relationship0302 clinical medicineHealth Information ManagementmedicinecraniosinostosisSurgical treatmentclinical surveybusiness.industryHealth Policylcsh:Rsubjective assessmentmedicine.diseaseFacial appearanceSkullmedicine.anatomical_structure030220 oncology & carcinogenesisresults of surgerybusiness030217 neurology & neurosurgeryHealthcare
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Dental approach for Apert syndrome in children : a systematic review

2017

Background Apert Syndrome (AS), or type I acrocephalosyndactyly, is a rare, congenital craniosynostosis condition resulting from missense mutations in the gene encoding fibroblast growth factor receptor 2. It is characterized by three specific clinical features: brachycephalic skull; midface hypoplasia, and limb abnormalities (syndactyly of hands and feet). The disorder exhibits variable presentations in bones, brain, skin, internal organs, and in the oral/maxillofacial region. The aim of the present paper was to show the main results from a systematic review of AS. Material and Methods A search of the literature was performed from April to June 2016 in five electronic databases. Clinical i…

Pediatricsmedicine.medical_specialtyMEDLINEReviewApert syndromeCraniosynostosis030207 dermatology & venereal diseases03 medical and health sciences0302 clinical medicinemedicineHumansSyndactylyChildDental CareGeneral DentistryOral Medicine and PathologyCochrane collaborationbusiness.industry030206 dentistryAcrocephalosyndactyliamedicine.disease:CIENCIAS MÉDICAS [UNESCO]Midface hypoplasiaSkullmedicine.anatomical_structureOtorhinolaryngologyUNESCO::CIENCIAS MÉDICASSurgeryObservational studybusiness
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Non-syndromic craniosynostosis in children : scoping review

2017

Background Craniosynostosis (CS) is a complex condition consisting of the early fusion of one or more cranial sutures in the intrauterine stage. The affected infant exhibits abnormal head shape at time of birth or shortly thereafter. It can be observed in normal individuals (non-syndromic CS or NSCS) or as a part of a multisystem syndrome. The purposes of the present article were to carry out a scoping review on Non-Syndromic CS and to discuss the most important findings retrieved. Material and Methods The steps of this scoping review were as follows: first, to pose a research question; second, to identify relevant studies to answer the research question; third, to select and retrieve the s…

Pediatricsmedicine.medical_specialtyMEDLINEReviewCochrane LibraryCraniosynostosesCraniosynostosis03 medical and health sciencesCraniosynostoses0302 clinical medicineHealth teamMedicineHumans030212 general & internal medicineChildGeneral DentistryResearch questionOral Medicine and Pathologybusiness.industry030206 dentistrymedicine.disease:CIENCIAS MÉDICAS [UNESCO]OtorhinolaryngologyUNESCO::CIENCIAS MÉDICASSurgeryOral health carebusinessNon syndromic
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