Cargando…

Oral manifestations of Ellis-van Creveld syndrome

Ellis-van Creveld syndrome is a rare autosomal-recessive disorder characterized by short limbs, post-axial polydactyly, ectodermal dysplasia, edentulous mandibular incisor region, absence of mucobuccal fold, congenitally missing teeth, slight serrations of the alveolar ridge and multiple small alveo...

Descripción completa

Detalles Bibliográficos
Autores principales:	Kalaskar, Ritesh, Kalaskar, Ashita R.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Medknow Publications & Media Pvt Ltd 2012
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3354796/ https://www.ncbi.nlm.nih.gov/pubmed/22629068 http://dx.doi.org/10.4103/0976-237X.95106

Ejemplares similares

Ellis–van Creveld
por: Jayaraj, Dhandabani, et al.
Publicado: (2012)

Oral manifestations of ellis-van creveld syndrome. A rare case report
por: Peña-Cardelles, Juan-Francisco, et al.
Publicado: (2019)

Ellis-Van Creveld syndrome
por: Baujat, Geneviève, et al.
Publicado: (2007)

Ellis Van Creveld Syndrome with Synpolydactyly, an Antenatal Diagnosis with Postnatal Correlation
por: Kundaragi, Nischal G, et al.
Publicado: (2011)

Classical oral manifestations of Dyke-Davidoff-Masson syndrome: a case report with review of the literature
por: Kalaskar, Ritesh, et al.
Publicado: (2018)

Ellis-van Creveld Syndrome: A Case Report
por: Singh, Subash, et al.
Publicado: (2012)

Ellis-van Creveld syndrome: A rare clinical entity
por: Kamal, Reet, et al.
Publicado: (2013)

Ellis-van Creveld Syndrome: Mutations Uncovered in Lebanese Families
por: Valencia, Maria, et al.
Publicado: (2015)

Ellis Van Creveld Syndrome: Cardiac Anomalies and Anesthetic Implications
por: Guha, Amrita, et al.
Publicado: (2023)

Ellis-van Creveld syndrome in an Indian child: a case report
por: Veena, K.M., et al.
Publicado: (2011)

Ellis van Creveld syndrome with unusual association of essential infantile esotropia
por: Das, D., et al.
Publicado: (2010)

Ellis–Van Creveld syndrome in siblings: A rare case report
por: Gokulraj, Sabitha, et al.
Publicado: (2016)

Ellis van Creveld syndrome in a Tunisian child revealed by an Eisenmenger syndrome
por: Ajmi, Houda, et al.
Publicado: (2015)

Growth charts for children with Ellis–van Creveld syndrome
por: Verbeek, Sabine, et al.
Publicado: (2010)

Ellis–van Creveld syndrome with unusual oral and dental findings: A rare clinical entity
por: Shaik, Sameeulla, et al.
Publicado: (2016)

Ellis-van Creveld Syndrome: A Rare Clinical Report of Oral Rehabilitation by Interdisciplinary Approach
por: Naqash, Talib Amin, et al.
Publicado: (2018)

Ellis-van Creveld with an Unusual Dental Anomaly: A Case Report
por: Nethan, Suzanne Tanya, et al.
Publicado: (2017)

Prenatal Diagnosis of Ellis–van Creveld Syndrome by Targeted Sequencing
por: Hao, Xiao-Yan, et al.
Publicado: (2016)

Marked Hypoplasia of the Distal Phalanges in Ellis–Van Creveld Syndrome
por: Marcelis, Stijn, et al.
Publicado: (2018)

Report of Two Siblings with Overlapping Features of Ellis-van Creveld and Weyers Acrodental Dysostosis
por: Shetty, Devi C., et al.
Publicado: (2012)

Oral mucormycosis in an 18-month-old child: a rare case report with a literature review
por: Kalaskar, Ritesh Rambharos, et al.
Publicado: (2016)

Novel large deletion involving EVC and EVC2 in Ellis–van Creveld syndrome
por: Sato, Hiroki, et al.
Publicado: (2022)

Molecular and clinical analysis of Ellis-van Creveld syndrome in the United Arab Emirates
por: Ali, Bassam R, et al.
Publicado: (2010)

Isolated tympanic plate fracture detected by cone-beam computed tomography: report of four cases with review of literature
por: Kalaskar, Ashita Ritesh, et al.
Publicado: (2017)

Hereditary sensory and autonomic neuropathy type V: Report of a rare case
por: Kalaskar, Ritesh, et al.
Publicado: (2015)

Successful Two-step Correction for Severe Genu Valgum in Ellis-van Creveld Syndrome: A Case Report
por: Kamada, Tomomi, et al.
Publicado: (2017)

Ellis‐van Creveld syndrome novel pathogenic variant in the EVC2 gene a patient from Turkey
por: Öztürk, Özden, et al.
Publicado: (2021)

Repair of double orifice mitral valve with an atrioventricular septal defect in a girl with Ellis–Van Creveld syndrome
por: Al‐Dairy, Alwaleed, et al.
Publicado: (2022)

Identification of Compound Heterozygous EVC2 Gene Variants in Two Mexican Families with Ellis–van Creveld Syndrome
por: Negrete-Torres, Nancy, et al.
Publicado: (2023)

A severe form of Ellis-van Creveld syndrome caused by novel mutations in EVC2
por: Ohashi, Ikuko, et al.
Publicado: (2019)

Multidisciplinary management of impacted central incisors due to supernumerary teeth and an associated dentigerous cyst
por: Kalaskar, Ritesh R., et al.
Publicado: (2011)

Maturogenesis of non-vital immature permanent teeth
por: Kalaskar, Ritesh R., et al.
Publicado: (2013)

Neuroblastoma in early childhood: A rare case report and review of literature
por: Kalaskar, Ritesh R., et al.
Publicado: (2016)

An operative approach to address severe genu valgum deformity in the Ellis-van Creveld syndrome
por: Weiner, Dennis S., et al.
Publicado: (2014)

Exotropia in a case of Ellis Van Creveld syndrome: A rare case report
por: Nayak, Swatishree, et al.
Publicado: (2022)

A homozygous EVC mutation in a prenatal fetus with Ellis–van Creveld syndrome
por: Wang, Jie, et al.
Publicado: (2023)

A Rare Clinical Variant of Oromandibular Limb Hypogenesis Syndrome Type I B
por: Kalaskar, Ritesh Rambharos, et al.
Publicado: (2016)

Molecular mechanisms of Ellis-van Creveld gene variations in ventricular septal defect
por: Liu, Fadi, et al.
Publicado: (2018)

Ellis–van Creveld Syndrome in Iran, a Case Report and Review of Disease Cases in Iran, Middle East
por: Baghianimoghadam, Behnam, et al.
Publicado: (2021)

Wide-spread cone-shaped epiphyses in two Saudi siblings with Ellis-van Creveld syndrome
por: Al-Fardan, Abeer, et al.
Publicado: (2017)

Cannot write session to /tmp/vufind_sessions/sess_6taie69mdcsk1a96vgvp36rse4