Browsing by Author "Callea M."
Now showing items 1-15 of 15
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Alagille Syndrome: A review
Callea M.; Bahsi E.; Montanari M.; Ince B.; Mancini G.E.; Yavuz Y.; Radovich F. (2013)Alagille Syndrome (AGS) is a genetically determined multisystem disorder affecting liver, hearth, eyes, skeleton and facies, less commonly kidney and CNS. The prognosis depends on the severity of the associated anomalies. ... -
Bifid uvula and submucous cleft palate in cornelia de lange syndrome
Callea M.; Montanari M.; Radovich F.; Clarich G.; Yavuz I. (2011)Cornelia de Lange syndrome is a rare congenital disease characterized by growth and psychomotor retardation, peculiar facial feature as skeletal and craniofacial deformities, gastrointestinal and cardiac problems and ... -
A c.3037G>a mutation in FBN1 gene causing marfan syndrome with an atypically severe phenotype
Callea M.; Willoughby C.E.; Camarata-Scalisi F.; Giovannoni I.; Vinciguerra A.; Yavuz I.; Di Stazio M. (Instituto de Investigaciones Clinicas, 2017)Marfan syndrome is a pleiotropic connective tissue disease inherited as an autosomal dominant trait, mostly caused by mutations in the FBN1 gene, which is located on chromosome 15q21.1 and encoding fibrillin 1. We report ... -
A case of Beckwith- Wiedemann syndrome with peculiar dental findings
Callea M.; Yavuz I.; Clarich G.; Gunay A.; Vinciguerra A.; Unal M.; Sahbaz C. (Ariesdue Srl, 2016)Background Beckwith-Wiedemann syndrome (BWS, OMIM 130650) is a rare genetic disorder characterised by overgrowth, tumor predisposition and congenital malformations. Few systemic manifestations and oral features have been ... -
Dental phenotype in a patient with hypoidrotic ectodermal dysplasia and severe immunodeficiency
Ectodermal dysplasia is a rare disease which affects at least two ectoderm-derived structures such as hair, nails, skin, sweat glands and teeth. The dentition is altered in number and shape. A 14-year-old male patient with ... -
Evaluation of root fracture in permanent teeth according to season
Dogan M.S.; Kusdhany L.S.; Maharani D.A.; Callea M.; Yavuz I. (Polskie Towarzystwo Stomatologiczne, 2017)Aim of the study. Root fractures which occur as a result of dental trauma may change according to school and holiday periods, and seasons. The aim of our study was to evaluate their incidence as dental trauma based on ... -
HED (Hypohidrotic Ectodermal Dysplasia): A Review
Callea M.; Scalisi F.C.; Yavuz I.; Dogan M.S.; Willoughby C.E.; Bashyam M.D. (University of Dicle, 2021)Abstract The ectodermal dysplasias (EDs) are a heterogeneous group of inherited, developmental disorders characterized by alterations in two or more ectodermal structures including the hair, teeth, nails and sweat glands. ... -
Hypohydrotic ectodermal dysplasia: A clinical case report
Callea M.; Paglia M.; Bahsi E.; di Stazio M.; Ince B.; Fedele G.; Yavuz Y. (University of Dicle, 2014)In times where rare diseases, mostly of genetic offspring, lead research to carry out genetic counselling to better understand the pathogenetic role of the diseases, with chances to develop alternative therapy respect than ... -
An interdisciplinary approach in a patient with amelogenesis imperfecta: A clinical report and literatüre review
Ulku S.Z.B.; Callea M.; Yavuz I.; Clarich G.; Kaya F.A.; Maglione M.; Kaya S. (2012)This clinical report describes an interdisciplinary approach for the coordinated treatment of a 20-year-old woman patient diagnosed with amelogenesis imperfecta. The treatment objective was to restore masticatory function, ... -
A new biological approach to guided bone and tissue regeneration
Montanari M.; Callea M.; Yavuz I.; Maglione M. (2013)The purpose of this study was to determine the potential of platelet-rich fibrin (PRF) membranes used for guided bone and tissue regeneration. A patient with insufficient alveolar ridge width in aesthetic zone was enrolled. ... -
A new phenotypic variant in cleidocranial dysplasia (CCD) associated with mutation c.391C>T of the RUNX2 gene
Callea M.; Fattori F.; Yavuz I.; Bertini E. (BMJ Publishing Group, 2012)The RUNX2 gene is a physiological regulatory gene implicated in the development of cleidocranial dysplasia (CCD). A 13-month-old child presented with clinical features of CCD. At the age of 3 years the diagnosis was ... -
Oral manifestation of Goltz-Gorlin syndrome in a young girl
Callea M.; Yavuz I.; Deroma L.; Montanari M.; Clarich G.; Maglione M.; Albertini E. (BioMed Central Ltd., 2012)[No abstract available] -
Oral manifestations in a boy with X-linked reticulate pigmentary disorder
Callea M.; Maglione M.; Yavuz I.; Deroma L.; Willoughby C.E.; Tadini G. (BioMed Central Ltd., 2012)[No abstract available] -
Syndromic craniosynostosis: A review
Cammarata-Scalisi F.; Ozen B.; Chacín J.A.; Yavuz I.; Callea M. (University of Dicle, 2016)Craniosynostosisis a defect of the skull caused by premature fusion of one or more cranial sutures. It may be isolated finding or part of a syndrome and affects 1 in every 2,500 live births.Usually multiple sutures are ... -
An unusual case: Neurofibromatosis type 5
Callea M.; Ulku S.Z.B.; Giustini S.; Yavuz I.; Ulku M.M.; Montanari M.; Basaran G. (2012)Neurofibromatosis is a disease which includes 5 types in its classification. It has been firstly described by Robert Smith in 1849, but its name comes from the first publication in 1882, in which Von Recklinghausen convinced ...
