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Oral Clefts with Associated Anomalies: Findings in the Hungarian Congenital Abnormality Registry [PDF]
, 2005 BACKGROUND: Over the years, great efforts have been made to record the frequency of orofacial clefts in different populations. However, very few studies were able to account for the etiological and phenotypic heterogeneity of these conditions. Thus, data
Czeizel, Andrew E. +2 more
core +3 more sources
A CASE REPORT: UNILATERAL COMPLETE CLEFT LIP RECONSTRUCTION USING THE MODIFICATION MILLARD TECHNIQUE
Jurnal Rekonstruksi dan Estetik, 2023 Highlights: • The modified Millard technique, including the Tennison triangular flap, is effective in preventing vermillion notching and reducing scar complications in cleft lip repairs.
Theodora Ratih Labdagati Iswara +1 more
doaj +1 more source
Electrophysiological assessment of auditory processing disorder in children with non-syndromic cleft lip and/or palate [PDF]
, 2015 Objectives Cleft lip and/or palate is a common congenital craniofacial malformation found worldwide. A frequently associated disorder is conductive hearing loss, and this disorder has been thoroughly investigated in children with non-syndromic cleft lip
Ma, LIAN, MA, X, McPherson, DB
core +4 more sources
Heliyon, 2023 Cleft palate (CP) is a common neonatal craniofacial defect caused by the adhesion and fusion dysfunction of bilateral embryonic palatal shelf structures. Long non-coding RNA (lncRNA) is involved in CP formation with regulatory mechanism unknown.
Ming Zhang +5 more
doaj
Feeding interventions for growth and development in infants with cleft lip, cleft palate or cleft lip and palate. [PDF]
, 2011 BACKGROUND: Cleft lip and cleft palate are common birth defects, affecting about one baby of every 700 born. Feeding these babies is an immediate concern and there is evidence of delay in growth of children with a cleft as compared to those without ...
Bessell, A +5 more
core +1 more source
Role of bone graft materials for cleft lip and palate patients: A systematic review [PDF]
, 1992 Cleft lip and palate is a congenital anomaly. Its management requires a long term commitment, multidisciplinary and structured treatment. Treatment is initiated at infancy and continues till adolescence.
Wahaj, Aiyesha +2 more
core +1 more source
The refinement of the median tubercle of cleft lip
Indian Journal of Plastic Surgery, 2018 Aim: Repair of cleft lip aims to bring symmetry and provide normal aesthetics for the lip. Several techniques have been employed; however, the finer aspect of median lip tubercle has not been emphasised in cleft lip repair. Materials and Methods: We have
Jyotsna Murthy
doaj +1 more source
Distinct DNA methylation profiles in subtypes of orofacial cleft [PDF]
, 2017 Background Epigenetic data could help identify risk factors for orofacial clefts, either by revealing a causal role for epigenetic mechanisms in causing clefts or by capturing information about causal genetic or environmental factors.
Davey Smith, George +9 more
core +2 more sources
Cholesteatoma and family history: An international survey [PDF]
, 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
Brazilian Journal of Otorhinolaryngology, 2021 Introduction: Non-syndromic cleft lip with or without cleft palate is a common worldwide birth defect due to a combination of environmental and genetic factors.
Qian Wang +5 more
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