Cargando…

Esthetic and functional rehabilitation in patients with cleft lip and palate

Oral rehabilitation of missing teeth in cleft patients has acceptable success rates. A two-stage approach is indicated; however, timing of implant placement in the grafted maxilla varies within existing protocols. This case highlights successful implant osseointegration and esthetic oral rehabilitat...

Descripción completa

Detalles Bibliográficos
Autores principales:	Bousdras, Vasilios A., Ayliffe, Peter R., Barrett, Mark, Hopper, Colin
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Medknow Publications & Media Pvt Ltd 2015
Materias:	Case Report - Developmental Defect
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4555933/ https://www.ncbi.nlm.nih.gov/pubmed/26389047 http://dx.doi.org/10.4103/2231-0746.161109

Ejemplares similares

Nasoalveolar molding in a case of incomplete cleft lip: Is it worth doing?
por: Esenlik, Elçin, et al.
Publicado: (2015)

Esthetic, Functional, and Everyday Life Assessment of Individuals with Cleft Lip and/or Palate
por: Gkantidis, Nikolaos, et al.
Publicado: (2015)

Nonsyndromic palate Synechia with floor of mouth
por: Naidoo, Sharan, et al.
Publicado: (2015)

Disruption of RAB40AL function leads to Martin–Probst syndrome, a rare X-linked multisystem neurodevelopmental human disorder
por: Bedoyan, Jirair Krikor, et al.
Publicado: (2012)

Biallelic NPR1 loss of function variants are responsible for neonatal systemic hypertension
por: Capri, Yline, et al.
Publicado: (2023)

MAB21L1 loss of function causes a syndromic neurodevelopmental disorder with distinctive cerebellar, ocular, craniofacial and genital features (COFG syndrome)
por: Rad, Abolfazl, et al.
Publicado: (2019)

Uncovering the burden of hidden ciliopathies in the 100 000 Genomes Project: a reverse phenotyping approach
por: Best, Sunayna, et al.
Publicado: (2022)

Biallelic ANGPT2 loss-of-function causes severe early-onset non-immune hydrops fetalis
por: Smeland, Marie F., et al.
Publicado: (2023)

Craniosynostosis, inner ear, and renal anomalies in a child with complete loss of SPRY1 (sprouty homolog 1) function
por: Tooze, Rebecca S, et al.
Publicado: (2023)

Esthetic Composition of Smile in Individuals with Cleft Lip, Alveolus, and Palate: Visibility of the Periodontium and the Esthetics of Smile
por: Esper, Luis Augusto, et al.
Publicado: (2012)

The kinetochore protein, CENPF, is mutated in human ciliopathy and microcephaly phenotypes
por: Waters, Aoife M, et al.
Publicado: (2015)

Facial profile esthetics in operated children with bilateral cleft lip and palate
por: Lauris, Rita de Cássia Moura Carvalho, et al.
Publicado: (2017)

Exome sequencing identifies mutations in the gene TTC7A in French-Canadian cases with hereditary multiple intestinal atresia
por: Samuels, Mark E, et al.
Publicado: (2013)

Diagnostic value of exome and whole genome sequencing in craniosynostosis
por: Miller, Kerry A, et al.
Publicado: (2017)

Mutations in CEP120 cause Joubert syndrome as well as complex ciliopathy phenotypes
por: Roosing, Susanne, et al.
Publicado: (2016)

A specific mutation in TBL1XR1 causes Pierpont syndrome
por: Heinen, Charlotte A, et al.
Publicado: (2016)

Phenotypic spectrum and genomics of undiagnosed arthrogryposis multiplex congenita
por: Laquerriere, Annie, et al.
Publicado: (2022)

Exome sequencing identifies DYNC2H1 mutations as a common cause of asphyxiating thoracic dystrophy (Jeune syndrome) without major polydactyly, renal or retinal involvement
por: Schmidts, Miriam, et al.
Publicado: (2013)

Segmental maxillary distraction with a novel device for closure of a wide alveolar cleft
por: Bousdras, Vasilios A., et al.
Publicado: (2014)

Cleft Lip and Palate
por: Pang, John, et al.
Publicado: (2013)

ARHGDIA: a novel gene implicated in nephrotic syndrome
por: Gupta, Indra Rani, et al.
Publicado: (2013)

FGFR1 mutations cause Hartsfield syndrome, the unique association of holoprosencephaly and ectrodactyly
por: Simonis, Nicolas, et al.
Publicado: (2013)

Genetic spectrum of Saudi Arabian patients with antenatal cystic kidney disease and ciliopathy phenotypes using a targeted renal gene panel
por: Al-Hamed, Mohamed H, et al.
Publicado: (2016)

Deletions and de novo mutations of SOX11 are associated with a neurodevelopmental disorder with features of Coffin–Siris syndrome
por: Hempel, Annmarie, et al.
Publicado: (2016)

Bicuspid aortic valve and aortic coarctation are linked to deletion of the X chromosome short arm in Turner syndrome
por: Bondy, Carolyn, et al.
Publicado: (2013)

Severity of oro-dental anomalies in Loeys-Dietz syndrome segregates by gene mutation
por: Jani, Priyam, et al.
Publicado: (2020)

‘Kinesinopathies’: emerging role of the kinesin family member genes in birth defects
por: Kalantari, Silvia, et al.
Publicado: (2020)

Familial bilateral cryptorchidism is caused by recessive variants in RXFP2
por: Ayers, Katie, et al.
Publicado: (2019)

Cornelia de Lange syndrome: from molecular diagnosis to therapeutic approach
por: Sarogni, Patrizia, et al.
Publicado: (2020)

DLG5 variants are associated with multiple congenital anomalies including ciliopathy phenotypes
por: Marquez, Jonathan, et al.
Publicado: (2021)

ARF1-related disorder: phenotypic and molecular spectrum
por: de Sainte Agathe, Jean-Madeleine, et al.
Publicado: (2023)

X-linked variations in SHROOM4 are implicated in congenital anomalies of the urinary tract and the anorectal, cardiovascular and central nervous systems
por: Kolvenbach, Caroline M, et al.
Publicado: (2023)

Primary care in early cleft lip and palate rehabilitation: A dental perspective
por: Ferreira, Amanda Nadia, et al.
Publicado: (2022)

Prosthodontic Rehabilitation Alternative of Patients with Cleft Lip and Palate (CLP): Two Cases Report
por: Ayna, Emrah, et al.
Publicado: (2009)

The maxillary lateral incisor in the rehabilitation of cleft lip and palate
por: Tereza, Guida Paola Genovez, et al.
Publicado: (2018)

Assessment of Folic Acid and DNA Damage in Cleft Lip and Cleft Palate
por: Brooklyin, Sivakumar, et al.
Publicado: (2014)

CLEFT LIP AND PALATE
Publicado: (1957)

CLEFT LIP AND PALATE
Publicado: (1963)

Rehabilitation of a One-day-Old Neonate with Cleft Lip and Palate using Palatal Obturator: A Case Report
por: Bansal, Rajesh, et al.
Publicado: (2012)

Developing a visual rating chart for the esthetic outcome of unilateral cleft lip and palate repair
por: Adeola, A. Olusanya, et al.
Publicado: (2015)

Cannot write session to /tmp/vufind_sessions/sess_9hdqtoufe8bd0pn0qcue8fljtq