• 대한두개안면성형외과학회지
• /
• 제18권1호
• /
• pp.71-71
• /
• 2017

• 대한두개안면성형외과학회지
• /
• 제16권1호
• /
• pp.47-47
• /
• 2015

• 대한두개안면성형외과학회지
• /
• 제19권4호
• /
• pp.311-311
• /
• 2018

• 대한두개안면성형외과학회지
• /
• 제23권6호
• /
• pp.282-283
• /
• 2022

• 대한두개안면성형외과학회지
• /
• 제22권6호
• /
• pp.345-345
• /
• 2021

• 대한두개안면성형외과학회지
• /
• 제20권6호
• /
• pp.425-425
• /
• 2019

• 대한두개안면성형외과학회지
• /
• 제24권6호
• /
• pp.292-292
• /
• 2023

• 대한구순구개열학회지
• /
• 제10권2호
• /
• pp.75-80
• /
• 2007

For the treatment of cleft palate patients, orthognathic surgery has been used by standard protocol. Predictable results have been achieved with standard techniques in slight to moderate maxillary hypoplasia. However, limited advancement and high relapse rate was reported in severe cases. The purpose of the present study was to review the clinical results of distraction osteogenesis in the patients with cleft lip and palate. Distraction osteogenesis has improved results in these patients by allowing soft tissue relaxation and gradual bone generation. Therefore, greater movement of the craniofacial skeleton is possible in severe cases of maxillary retrusion with lower relapse rates. In conclusion, distraction osteogenesis for the advancement of hypoplastic maxilla of cleft patients has shown successful treatment method.

• 대한구순구개열학회지
• /
• 제3권1호
• /
• pp.33-36
• /
• 2000

Cornelia de Lange syndrome is a disorder of unknown biochemical and geneic basis that is recognized on the basis of characteristic facies(low anterior hairline, synophrys, anteverted nares, maxillary prognathism, long philtrum, carp mouth) in association with prenatal and postnatal growth retardation, mental retardation and, in many cases, upper limb anomalies. We treated the patient with incomplete cleft palate related to Cornelia de Lange syndrome.

• 대한구순구개열학회지
• /
• 제11권2호
• /
• pp.59-63
• /
• 2008

Craniofacial Centre at Children's Hospital Boston is a worldwide leader in the care of children and adolescents with craniofacial anomalies especially with cleft lip and/or cleft palate, which provides a team approach to the evaluation, diagnosis and treatment of children and adults with congenital (present at birth) or acquired facial deformities. This is staffed by an experienced team of clinicians, such as in oral and maxillofacial surgery, plastic surgery, neurosurgery, dentistry, audiology, speech and language pathology, genetics, psychiatry, otolaryngology, and social work, all with specialized training in the care of children with craniofacial anomalies. Here, there is a short introduction of history, attending surgeons, works, and sequential treatment for cleft lip/palate patients about this institution.