Results 11 to 20 of about 50,330 (260)

Cholesteatoma and family history: An international survey [PDF]

open access: yes, 2020
Objective To explore the relative frequency of a family history of cholesteatoma in patients with known cholesteatoma, and whether bilateral disease or earlier diagnosis is more likely in those with a family history.
Clark, Allan   +6 more
core   +1 more source

MODIFIED CLEFT LIP EVALUATION PROFILE (MCLEP) INDEX FOR UNILATERAL CLEFT LIP REPAIR OUTCOME ASSESSMENT IN SURABAYA CLP CENTER

open access: yesJurnal Rekonstruksi dan Estetik, 2020
Highlights: • The study revealed that there were no notable variations in the ultimate scores, regardless of whether the cleft lip was complete or an alveolar cleft was present.
Robertus Arian Datusanantyo   +2 more
doaj   +1 more source

Beware of Optical Illusion of the Alar Base in Unilateral Cleft Lip Nasal Deformity

open access: yesPlastic and Reconstructive Surgery, Global Open, 2021
Background:. It is generally accepted that the alar base on the cleft side in the cleft lip nose is displaced outward and downward; therefore, it is rotated inward and upward in almost all procedures for cleft lip closure.
Yoshiaki Sakamoto, MD   +2 more
doaj   +1 more source

Assessment of facial asymmetry before and after the surgical repair of cleft lip in unilateral cleft lip and palate cases [PDF]

open access: yes, 2018
This study was performed to assess facial asymmetry in patients with unilateral cleft lip and palate (UCLP) before and after primary lip repair. Three-dimensional facial images of 30 UCLP cases (mean age 3.7 ± 0.8 months) captured 1–2 days before surgery
Al-Rudainy, D.   +3 more
core   +1 more source

A case report of acampomelic campomelic dysplasia and operative difficulties in cleft palate reconstruction

open access: yesIndian Journal of Plastic Surgery, 2016
Acampomelic campomelic dysplasia (CD) is a type of CD (CD; OMIM #114290), a rare form of congenital short-limbed dwarfism and is due to mutations in SOX9 gene family.
M. Pasupathy   +3 more
doaj   +1 more source

Dental Implant Treatment for a Patient with Bilateral Cleft Lip and Palate [PDF]

open access: yes, 2008
Dental reconstruction in the cleft space is difficult in some patients with cleft lip and palate because of oronasal fistulas. Most of these patients receive a particle cancellous bone marrow (PCBM) graft to close the alveolar cleft, and secondary bone ...
Honda, Kozo   +7 more
core   +1 more source

Prevalence of cleft lip and palate in Bauru, SP – concordance among registries of HRAC/USP, DNV and SINASC

open access: yesBrazilian Dental Science, 2021
Objective: Congenital defects, including cleft lip and palate, increase the morbidity and mortality in the affected population. This study aimed to determine the prevalence of cleft lip and palate in the city of Bauru, Brazil, by evaluation of registry ...
Kelly Fernanda Molena   +2 more
doaj   +1 more source

Health professional communication and the diagnosis and care of infants born with cleft lip and palate in the U.K. [PDF]

open access: yes, 2016
Objectives A qualitative study was conducted to explore family experiences of communication with health care professionals following the diagnosis and birth of a child with cleft lip and/or palate in the United Kingdom.
Ryan, Sara   +2 more
core   +3 more sources

Profile of post operative cleft lip and palate in aceh cleft lip and palate center period of November 2018 - October 2019

open access: yesJKS (Jurnal Kedokteran Syiah Kuala), 2022
Cleft Lip and Cleft Palate or Orofacial Cleft, which is known as the cleft lip is a condition of birth defects where an unusual opening or cleft is formed on the lips or palate.1 Cleft lip or labioschisis is a congenital anomaly that formed in the first ...
Syamsul Rizal   +4 more
doaj   +1 more source

Tessier number 30 clefts with congenital heart defects [PDF]

open access: yes, 2015
Introduction: Midline cleft of mandible, classified as Tessier 30 clefts is extremely rare, with less than 100 reported cases in the latest studies. Variations in severity and associated malformations have been reported before. Case Presentation: In this
Aminolsharieh Najaf, S.   +4 more
core   +1 more source

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