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Intranasal teeth in a 3-year-old child with Smith-Lemli-Opitz syndrome

Shim SH

Smith–Lemli–Opitz syndrome (SLOS) is a rare autosomal recessive genetic disorder accompanied with congenital anomalies and mental impairment. Clefts of the hard and/or soft palate, small tongue, broad alveolar ridges, and...
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Early outcomes of cleft and palatal width following anterior palate repair (vomerine flap) in infants with wide cleft lip and palate

Mat Saad A, Chai KS, Wan Sulaiman WA, Mat Johar , Halim AS

BACKGROUND: Anterior palatal repair performed during cleft lip repair using a vomerine flap may assist in recruiting additional soft tissue for subsequent completion of palatoplasty, especially in patients with a...
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Establishing cleft services in developing countries: Complications of cleft lip and palate surgery in rural areas of Indonesia

Ruslin M, Dom L, Tajrin A, Hajrah Yusuf AS, Arif SK, Tanra AH, Ou KL, Forouzanfar T, Thamrin SA

BACKGROUND: Cleft treatment is frequently performed in Indonesia, mostly in charity missions, but without a postoperative protocol it is difficult to establish the risks and complications of cleft treatment. The...
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Comparison of minimally invasive versus conventional open harvesting technique for iliac bone graft in secondary alveolar bone grafting in cleft palate patients: a systematic review

Saha A, Shah S, Waknis P, Bhujbal P, Aher S, Vaswani V

This study evaluated and compared the donor site morbidity following minimally invasive and conventional open harvesting of iliac bone for secondary alveolar bone grafting in cleft palate patients. A thorough...
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Soft tissue reconstruction in wide Tessier number 3 cleft using the straight-line advanced release technique

Kim GH, Baek RM, Kim BK

Craniofacial cleft is a rare disease, and has multiple variations with a wide spectrum of severity. Among several classification systems of craniofacial clefts, the Tessier classification is the most widely...
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Concurrent SHORT syndrome and 3q duplication syndrome

Boaz AM, Grasso SA, DeRogatis , Beesley EN

SHORT syndrome is an extremely rare congenital condition due to a chromosomal mutation of the PIK3R1 gene found at 5q13.1. SHORT is a mnemonic representing six manifestations of the syndrome:...
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Treatment of velopharyngeal insufficiency in a patient with a submucous cleft palate using a speech aid: the more treatment options, the better the treatment results

Park YH, Jo HJ, Hong IS, Leem DH, Baek JA, Ko SO

BACKGROUND: The submucous cleft palate (SMCP) is a type of cleft palate that may result in velopharyngeal insufficiency (VPI). Palate muscles completely separate oral and nasal cavities by closing off...
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Surgical correction for Tessier number 7 craniofacial cleft using a medially overcorrected design

Ryu JY, Eo PS, Tian L, Lee JS, Lee JW, Choi KY, Yang JD, Chung HY, Cho BC

BACKGROUND: Various surgical techniques have been used to correct Tessier number 7 craniofacial cleft, which involves macrostomia, ear deformity, and hemifacial microsomia. To achieve symmetrical and satisfactory results in patients...
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Prenatal ultrasonography of craniofacial abnormalities

Mak AS, Leung KY

Craniofacial abnormalities are common. It is important to examine the fetal face and skull Epub ahead of print during prenatal ultrasound examinations because abnormalities of these structures may indicate the...
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Prosthetic treatment for patient with congenital bilateral cleft lip and palate to close oro-nasal communication using maxillary double crown and clasp retained removable denture

Doh SJ, Cho JH

Patients with cleft lip and palate have several problems such as oro-nasal communication, dental cross-bite caused by the insufficient growth of maxilla, poor pronunciation and esthetic problem. Removable denture with...
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Airway management in pediatric tongue flap division for oronasal fistula closure: A case report

So E, Yun HJ, Karm MH, Kim HJ, Seo KS, Ha H

Oronasal fistulae (ONF) could remain after surgery in some patients with cleft palate. ONF ultimately requires intraoral surgery, which may lead to perioperative airway obstruction. Tongue flap surgery is a...
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A Rare Case of Hyponatremia Caused by Reset Osmostat in a Neonate with Cleft Lip, Cleft Palate, and Imperforate Anus

Ahn JG, Lee JE, Chung WY, Koo SH, Shin J, Jeon GW

Hyponatremia is defined as a plasma sodium concentration of < 135 mEq/L. It is a common electrolyte imbalance in newborns. We report the case of a term neonate with cleft...
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Trend of health care utilization of cleft lip and/or palate in Korea during 2007–2016

Hong M, Baek SH

OBJECTIVE: This study is performed to investigate the trend of health care (HC) utilization among cleft lip and/or palate (CL/P) during 2007–2016 by using data from the Korean National Health...
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Optimal Xeno-free Culture Condition for Clinical Grade Stem Cells from Human Exfoliated Deciduous Teeth

Tangjit N, Dechkunakorn S, Anuwongnukroh N, Khaneungthong A, Sritanaudomchai H

BACKGROUND AND OBJECTIVES: Stem cells from human exfoliated deciduous teeth (SHED) are a promising clinical resource for various tissue defects, including lumbar spondylosis, neural compression, and cleft palate. Use of...
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Comparative study of levobupivacaine and bupivacaine for bilateral maxillary nerve block during pediatric primary cleft palate surgery: a randomized double-blind controlled study

Mostafa MF, Herdan R, Elshazly M

BACKGROUND: Cleft lip and palate are common major congenital anomalies. Cleft palate (CP) repair causes pain and needs large doses of intravenous opioids. The risk of postoperative airway obstruction or...
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Modified two flap palatoplasty in asymptomatic transsphenoidal encephalocele: a case report

Richardson S, Khandeparker RV, Raghuvaram AK, Mohan R

About one-third of patients with transsphenoidal basal encephaloceles have associated congenital anomalies, including cleft palate. Moreover, they are often plagued by symptomatic exacerbations in the form of upper respiratory obstructions,...
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A Case of Platyspondylic Lethal Skeletal Dysplasia Torrance Type

Lee SC, Choi MS

Platyspondylic lethal skeletal dysplasia, Torrance type (PLSD-T), is one of the phenotypes of type II collagenopathy and is characteristic of severe bone growth disorder. This phenotype may limit the growth...
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Investigation of postoperative hypernasality after superiorly based posterior pharyngeal flap

Shin YJ, Kim Y

BACKGROUND: Velopharyngeal insufficiency that accompanies speech resonance and articulation disorders can be managed through several intervention methods such as speech-language therapy, prosthetic aids, and surgery. However, for patients with severe...
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Anatomical repair of a bilateral Tessier No. 3 cleft by midfacial advancement

Oh JH, Park YW

BACKGROUND: Bilateral Tessier number 3 clefts are extremely rare, and their surgical treatments have not been well established. CASE PRESENTATION: The authors describe the case of a patient with a right...
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Treatment of the cleft lip and palate patient with few remaining posterior teeth using hybrid telescopic crown denture

Park JW, Cho JH

For individuals with cleft lip and palate, the removable partial dentures (RPDs) have been an important treatment option. Some modifications from conventional prosthetic treatment may be necessary to achieve satisfactory...
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