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Cleft Palate-craniofacial Journal

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https://www.readbyqxmd.com/read/28471735/clinical-finding-and-management-of-12-orofacial-clefts-cases-with-nevoid-basal-cell-carcinoma-syndrome
#1
Lee Mui Lee, Lian Ma, Tie Jun Li
Objective  To study the phenotype and overview the clinical management on Cleft Lip and/or Palate (CL/P) with Nevoid Basal Cell Carcinoma Syndrome (NBCCS) patients in Peking University School and Hospital of Stomatology. Design  Case series study. Main Outcome Measures  To describe the clinical phenotype of 12 CL/P with NBCCS patients who fulfilled the diagnostic criteria as well as to explore clinical management. Results  Seven cases (7/12, 58.33%) were classified as bilateral complete cleft lip and palate (BCCLP)...
May 2017: Cleft Palate-craniofacial Journal
https://www.readbyqxmd.com/read/28471734/acpa-s-74th-annual-meeting
#2
(no author information available yet)
No abstract text is available yet for this article.
May 2017: Cleft Palate-craniofacial Journal
https://www.readbyqxmd.com/read/28471733/acpa-2017-oral-presentation-abstracts
#3
(no author information available yet)
The peer-reviewed abstracts presented at the 74th Annual Meeting of the ACPA are published as submitted by the authors. For financial conflict of interest disclosure, please visit http://meeting.acpa-cpf.org/disclosures.html.
May 2017: Cleft Palate-craniofacial Journal
https://www.readbyqxmd.com/read/27259005/cleft-palate-and-aglossia-result-from-perturbations-in-wnt-and-hedgehog-signaling
#4
Gongjie Yuan, Gurpreet Singh, Serafine Chen, Kristy Carrington Perez, Yan Wu, Bo Liu, Jill Ann Helms
OBJECTIVE:   The objective of this study was to explore the molecular basis for cleft secondary palate and arrested tongue development caused by the loss of the intraflagellar transport protein, Kif3a. DESIGN:   Kif3a mutant embryos and their littermate controls were analyzed for defects in facial development at multiple stages of embryonic development. Histology was employed to understand the effects of Kif3a deletion on palate and tongue development. Various transgenic reporter strains were used to understand how deletion of Kif3a affected Hedgehog and Wnt signaling...
May 2017: Cleft Palate-craniofacial Journal
https://www.readbyqxmd.com/read/27115563/response-to-older-adults-experiences-of-living-with-cleft-lip-and-palate-a-qualitative-study-exploring-ageing-and-appearance
#5
Claire Hamlet, Diana Harcourt
No abstract text is available yet for this article.
May 2017: Cleft Palate-craniofacial Journal
https://www.readbyqxmd.com/read/27115562/interferon-regulatory-factor-6-controls-proliferation-of-keratinocytes-from-children-with-van-der-woude-syndrome
#6
Katherine Hixon, Lindsey Rhea, Jennifer Standley, Frank J Canady, John W Canady, Martine Dunnwald
OBJECTIVE:   Interferon Regulatory Factor 6 (IRF6) is critical for craniofacial development, epidermal differentiation, and tissue repair. IRF6 mutations cause Van der Woude Syndrome (VWS) and Popliteal Pterygium Syndrome. Individuals with VWS exhibit craniofacial anomalies, including cleft lip and palate and lip pits. Furthermore, they have an increased risk for wound-healing complications following surgical repair when compared with patients with nonsyndromic cleft lip and palate (NSCLP)...
May 2017: Cleft Palate-craniofacial Journal
https://www.readbyqxmd.com/read/27043654/breast-milk-feeding-rates-in-patients-with-cleft-lip-and-palate-at-a-north-american-craniofacial-center
#7
Michael Alperovich, Jordan D Frey, Pradip R Shetye, Barry H Grayson, Raj M Vyas
OBJECTIVE:   Our study goal was to evaluate the rates of breast milk feeding among patients with oral clefts at a large North American Craniofacial Center. METHODS:   Parents of patients with oral clefts born from 2000 to 2012 and treated at our center were interviewed regarding cleft diagnosis, counseling received for feeding, and feeding habits. RESULTS:   Data were obtained from parents of 110 patients with oral clefts. Eighty-four percent of parents received counseling for feeding a child with a cleft...
May 2017: Cleft Palate-craniofacial Journal
https://www.readbyqxmd.com/read/27043653/computed-tomographic-estimation-of-particulate-cancellous-bone-and-marrow-weight-for-successful-transplant-in-unilateral-cleft-lip-and-palate-patients
#8
Hiroshi Watanabe, Kenichi Kurita, Atsushi Nakayama, Eri Umemura, Masaki Ogita, Mitsuo Goto, Eiichiro Ariji
OBJECTIVE:   The defect volume measured on computed tomography (CT) for secondary bone graft (SBG) is well correlated to the actual amount of particulate cancellous bone and marrow (PCBM) transplanted in unilateral cleft lip and palate (UCLP) patients. However, the validity of such measurements have not been completely verified due to lack of evaluation of treatment results. The objective of this study was to propose an estimation method by CT based on the data of successfully treated patients...
May 2017: Cleft Palate-craniofacial Journal
https://www.readbyqxmd.com/read/27043651/influence-of-standardized-orientation-on-patient-perception-of-perioperative-care-following-alveolar-cleft-repair-a-survey-based-study-of-patients-treated-in-a-large-academic-medical-center
#9
Brian L Chang, Anthony J Wilson, Bianca C Chin, Christopher Friedman, Oksana A Jackson
OBJECTIVE:   This study aims to better understand patient-reported outcomes for iliac bone grafting surgery for alveolar cleft repair and to determine how standardizing perioperative patient instruction affects patient-reported outcomes. DESIGN:   Retrospective survey-based assessment of patients undergoing iliac bone grafting with and without hospital-based systems standardization. SETTING:   Academic tertiary care hospital. PATIENTS:   Of the 195 identified patients, 127 participated...
May 2017: Cleft Palate-craniofacial Journal
https://www.readbyqxmd.com/read/27043650/neurological-development-of-children-with-isolated-robin-sequence-treated-with-nasopharyngeal-intubation-in-early-infancy
#10
Tatiane Romanini Rodrigues Alencar, Ilza Lazarini Marques, Alvaro Bertucci, Rosana Prado-Oliveira
The study assessed the neurodevelopment of children with isolated Robin sequence (IRS) and evaluated if children treated exclusively with nasopharyngeal intubation (NPI) present delay in neurological development. The prospective and cross-sectional study was conducted at the Hospital for Rehabilitation of Craniofacial Anomalies, Brazil. Children with IRS were divided into two groups according to the type of treatment in early infancy: 38 were treated with NPI (more severe cases) and 24 with postural treatment (less severe cases)...
May 2017: Cleft Palate-craniofacial Journal
https://www.readbyqxmd.com/read/27031270/children-s-attitudes-toward-peers-with-unintelligible-speech-associated-with-cleft-lip-and-or-palate
#11
Alice Lee, Fiona E Gibbon, Kimberley Spivey
OBJECTIVE:   The objective of this study was to investigate whether reduced speech intelligibility in children with cleft palate affects social and personal attribute judgments made by typically developing children of different ages. DESIGN:   The study (1) measured the correlation between intelligibility scores of speech samples from children with cleft palate and social and personal attribute judgments made by typically developing children based on these samples and (2) compared the attitude judgments made by children of different ages...
May 2017: Cleft Palate-craniofacial Journal
https://www.readbyqxmd.com/read/27031269/a-longitudinal-study-of-the-presence-of-dental-anomalies-in-the-primary-and-permanent-dentitions-of-cleft-lip-and-or-palate-patients
#12
Akira Suzuki, Masayuki Nakano, Keigo Yoshizaki, Atsushi Yasunaga, Naoto Haruyama, Ichiro Takahashi
OBJECTIVE:   The aim is to survey primary and permanent dental anomalies: hypodontia, microdontia, a supernumerary tooth, and fused teeth in patients with cleft lip and/or palate. DESIGN:   Retrospective longitudinal study Subjects :  The subjects were selected from all 1724 patients with cleft lip and/or palate who were registered at the orthodontic clinic of Kyushu University Hospital, Fukuoka, Japan, from 1970 to 2009. Finally, 994 subjects were evaluated for primary dentition, 1352 for permanent dentition, and 871 for the longitudinal changes from primary to permanent dentition...
May 2017: Cleft Palate-craniofacial Journal
https://www.readbyqxmd.com/read/27031267/de-novo-1-77-mb-microdeletion-of-10q22-2q22-3-in-a-girl-with-developmental-delay-speech-delay-congenital-cleft-palate-and-bilateral-hearing-impairment
#13
Ting-Ying Lei, Hong-Tao Wang, Fan Li, Ying-Qiu Cui, Fang Fu, Ru Li, Can Liao
Interstitial deletions of chromosome band 10q22.1q22.3 are rare. We here report a 2.5-year-old female patient with developmental delay, speech delay, congenital cleft palate, and bilateral hearing impairment. The girl's karyotype was normal. Chromosome microarray analysis (CMA) revealed a 1.77-Mb de novo interstitial deletion in 10q22.2q22.3. The deletion harbors 9 genes, including KAT6B, DUPD1, DUSP13, SAMD8, VDAC2, COMTD1, ZNF503, NCRNA00245, and C10orf11. This is the first patient with a deletion of the smallest size in 10q22...
May 2017: Cleft Palate-craniofacial Journal
https://www.readbyqxmd.com/read/27031266/outcomes-of-44-consecutive-complete-bilateral-cleft-lip-and-palate-patients-treated-with-secondary-alveolar-bone-grafting-and-premaxillary-osteotomy
#14
Rupert Scott, Julia Scott, Sami Stagnell, Steve Robinson, Tim Flood
OBJECTIVE:   To report the surgical outcomes of secondary alveolar bone grafting with premaxillary osteotomy in a single surgeon cohort of complete bilateral cleft lip and palate patients. DESIGN:   Retrospective review of 44 consecutive patients using hospital notes and radiographs. SETTING:   Single specialist cleft lip and palate center, UK. PATIENTS:   Consecutive patients with complete bilateral cleft lip and palate who were being treated with secondary alveolar bone grafting incorporating premaxillary osteotomy...
May 2017: Cleft Palate-craniofacial Journal
https://www.readbyqxmd.com/read/26882026/tooth-abnormalities-and-occlusal-disorders-in-individuals-with-frontonasal-dysplasia
#15
Vanessa Benetello Dainezi, Lucimara Teixeira das Neves, Gisele da Silva Dalben, Marcia Ribeiro Gomide
OBJECTIVE:   Frontonasal dysplasia is a rare developmental defect of the midface, and little is known about the dental involvement in individuals with this condition. This study investigated tooth abnormalities and occlusal disorders in individuals with frontonasal dysplasia. DESIGN:   Cross-sectional. SETTING:   Hospital for Rehabilitation of Craniofacial Anomalies, University of São Paulo, Bauru, Brazil. INTERVENTIONS:   Clinical oral examination, analysis of patient records, and panoramic radiographs...
May 2017: Cleft Palate-craniofacial Journal
https://www.readbyqxmd.com/read/26752252/fetal-development-of-human-oral-epithelial-pearls-with-special-reference-to-their-stage-dependent-changes-in-distribution
#16
Ji Hyun Kim, Zhe Wu Jin, Shunichi Shibata, Jae Do Yang, Gen Murakami, José Francisco Rodríguez-Vázquez, Baik Hwan Cho
OBJECTIVE:   To access detailed distribution and age-dependent changes of oral epithelial pearls. DESIGN:   Investigation and analysis with human fetal serial sections. SETTING:   Institute of Embryology. METHODS:   This study examined serial frontal sections of the upper and lower jaws of 19 human fetuses at 12 to 18 weeks and of the lower jaws of four late-stage fetuses. RESULTS:   The upper jaw contained more than 20 midline and more than 60 lateral pearls greater than 20 μm in diameter, whereas the lower jaw contained fewer than 30 pearls of the same size...
May 2017: Cleft Palate-craniofacial Journal
https://www.readbyqxmd.com/read/26575965/lateral-soft-palate-growth-deficiency-case-report-and-therapeutic-management
#17
Luo Dongyuan, Chen Yiyang, Li Fan, Hao Jiansuo
We report the case of a girl with syndromic cleft palate, probably as part of a first branchial arch syndrome, who was unique in having almost complete unilateral aplasia of the soft palate. Rather than using soft tissue transplants or a prosthesis, we pioneered the use of a modified Furlow technique, which proved to be simple to perform, effective, and safe.
May 2017: Cleft Palate-craniofacial Journal
https://www.readbyqxmd.com/read/26506047/antenatal-ultrasound-detection-of-cleft-in-western-australia-from-2003-to-2012-a-follow-up-study
#18
W Nicholls, R Jennings, Y Yeung, M Walters, B Hewitt
AIM:   To investigate trends in the rate of antenatal detection of cleft lip and palate (CLP) patients referred to the CLP Unit at Princess Margaret Hospital for Children in Perth, Western Australia during the period 2003-2012 and compare data with a previously published report covering the years 1996-2003. METHODS:   This is a single-center, retrospective survey of antenatal transabdominal ultrasound screenings of mothers of infants born between July 1, 2003 and June 30, 2012 that were referred to the CLP Unit at Princess Margaret Hospital...
May 2017: Cleft Palate-craniofacial Journal
https://www.readbyqxmd.com/read/26237188/orthodontic-treatment-and-long-term-management-of-a-patient-with-marfan-syndrome
#19
Momotoshi Shiga, Takuya Ogawa, Issareeya Ekprachayakoon, Keiji Moriyama
Marfan syndrome (MFS) is caused by abnormal systemic connective tissue. The main clinical manifestations include long limbs, long slender fingers, lens subluxation, abnormal cardiac valves, and aortic aneurysm. We report the case of an 11-year-old patient with MFS who underwent orthodontic treatment and was followed up until the age of 25 years. We found no significant differences in tooth movement between the patient with MFS and healthy subjects. However, because patients with MFS show characteristic facial growth and an increased risk of developing systemic comorbidities, their dental status requires careful observation over time...
May 2017: Cleft Palate-craniofacial Journal
https://www.readbyqxmd.com/read/26068386/isolated-unilateral-soft-palate-palsy-following-tonsillopharyngitis-caused-by-epstein-barr-virus-infection
#20
Richie Gupta, Rajat Gupta, Sameer Sethi, Manoj Khanal
Soft palate palsy with or without pharyngeal or laryngeal paralysis or facial palsy has been described in the literature fewer than 40 times. Of these cases, isolated unilateral soft palate palsy (occurring without any other neurologic manifestation) has been rare. Most cases of isolated soft palate palsy were termed idiopathic in the past. In a few cases, a concomitant viral infection such as varicella zoster, herpes simplex, measles, and coxsackie A9 was diagnosed. We describe a case of isolated soft palate palsy, following a pharyngotonsillitis caused by Epstein-Barr virus...
May 2017: Cleft Palate-craniofacial Journal
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