Results 21 to 30 of about 38,765 (271)
Annals of Abbasi Shaheed Hospital and Karachi Medical & Dental College, 2021 Objective: To evaluate the patterns of cleft lip and palate by its type, side, gender, laterality and extent of involvement of hard and/or soft palate in patients reported to a tertiary care hospital in Karachi.
Zubair Ahmed Abbasi +4 more
doaj +1 more source
Primary unilateral cleft lip repair
Indian Journal of Plastic Surgery, 2009 The unilateral cleft lip is a complex deformity. Surgical correction has evolved from a straight repair through triangular and quadrilateral repairs to the Rotation Advancement Technique of Millard.
H. S. Adenwalla, P. V. Narayanan
doaj +1 more source
JKS (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
Cleft of lip and palate: A review
Journal of Family Medicine and Primary Care, 2020 Cleft of lip and palate are most common serial congenital anomalies to affect the orofacial region . It can occur isolated or together in various combination and/or along with other congenital deformities particularly congenital heart diseases. .Patient with oro-facial cleft deformity needs to be treated at right time and at right age to achieve ...
Sachin Kumar +5 more
openaire +4 more sources
BMJ Open, 2021 Objectives This study aimed to investigate the temporal and spatial characteristics of cleft lip and/or palate based on a large-scale birth defect monitoring database.Methods Data on perinatal infants and children with cleft lip and/or palate defects ...
Pi Guo +9 more
doaj +1 more source
Cleft Lip and Palate Treatment [PDF]
Plastic Surgery International, 2013 Cleft lip and palate is still a very challenging facial deformity, and this special issue has shown this very clearly. Many papers came from all around the world, and the topics were very up to date and have raised very interesting points. The topics about humanitarian mission and its role and the benefits are elucidated in these articles, but the ...
Luiz Bermudez +3 more
openaire +3 more sources
Trisomy 5p: Long Recognized, Rarely Published‐ Three New Cases and Review of the Literature
American Journal of Medical Genetics Part A, EarlyView.ABSTRACT Complete trisomy 5p is a rare chromosomal disorder caused by a duplication of the short arm of chromosome 5. Current data suggest that complete trisomy 5p presents as a distinct clinical syndrome including but not limited to seizures, developmental delays, facial dysmorphisms, failure to thrive, and recurrent respiratory infections.
Gabriela J. Kim +2 more
wiley +1 more source
Mortality Patterns and Phenotypic Clusters in Trisomy 13: A Population‐Based Study From Japan
American Journal of Medical Genetics Part A, EarlyView.ABSTRACT Trisomy 13, the third most common autosomal trisomy after trisomy 21 and trisomy 18, is associated with a significantly high infant mortality rate. However, large‐scale studies examining causes of death in trisomy 13 remain scarce. Therefore, we aimed to better understand the mortality patterns.
Narumi Kato +2 more
wiley +1 more source
De Novo Heterozygous ZFX Frameshift Variant in a Female With an X‐Linked Neurodevelopmental Disorder
American Journal of Medical Genetics Part A, EarlyView.ABSTRACT Germline ZFX variants are associated with an X‐linked neurodevelopmental disorder, with 14 males and 16 females reported to date. We describe a 20‐year‐old female with a heterozygous ZFX frameshift variant, p.(Met666Valfs*2), identified by genome sequencing, previously reported in an affected male.
Iftekhar A. Showpnil +8 more
wiley +1 more source
Journal of Indian Society of Pedodontics and Preventive Dentistry, 2011 Background: Cleft lip and palate is a common congenital defect. It is one of the most common facial deformities occurring in major racial and ethnic groups.
V Krishna Priya +3 more
doaj +1 more source