craniofacial  anomalies  include  clefts,  synostoses,  atrophic  abnormalities,neoplasias etc. among which cleft lip and/or palate caused by abnormal facial development during gestation is one of the most prevalent congenital defects. its overall occurrence is about 1:700 ranging from 0.02 to 4.04 in 1000 live births. there are different etiologic factors considering the cleft cause. in most c...

In this paper, based on Chinese data, I propose that the so called light verb construction can be subsumed under the analysis of internal topicalization, following the analysis of remnant movement. First, I argue that a light verb does assign theta-roles. Second, I argue that all the particular syntactic behaviors observed in Grimshaw and Mester (1988) the verbal noun cannot undergo topicalizat...

(2001) Genetic heterogeneity and exclusion of a modifying locus at 17p11.2-p11.1 in Finnish families with van der Woude syndrome. (2001) Mapping of the second locus for the Van der Woude syndrome to chromosome 1p34. (2003) Collagen XI sequence variations in nonsyndromic cleft palate, Robin sequence and micrognathia. (2003) Linkage and linkage disequilibrium searched between non-syndromic cleft ...

background oral cleft is the most common orofacial congenital anomaly among live births. this anomaly at birth is one of the main causes of children disability and mortality.  congenital heart disease (chd) is one of the most common anomalies in oral clefts.  this study aimed to assess the incidence of congenital heart diseases anomalies in newborns with oral clefts. materials and methods this ...

purpose: to report a case of hypotonous maculopathy after blunt trauma and its treatment. patient and findings: a 34-year-old woman presented with decreased visual acuity in her left eye following blunt trauma. right eye examination was unremarkable, but visual acuity of left eye was counting fingers. slit lamp biomicroscopy of the left eye was within normal limits, but on funduscopy, papilloma...

introduction: tessier facial cleft is among the rarest facial clefts reported in literatures and there are many issues arguing about its multidisciplinary repairing techniques. tessier number 4 and 5 are extremely rare facial anomalies. there are few literatures describing these clefts and their surgical modalities. number 5 tessier cleft begins medial to oral commissure in the upper lip and ex...

Neurocognitive disorders may compromise the outcome of surgical cleft lip palate repair and thus need to be identified. Processing of rapidly changing sequential information (temporal processing) is a fundamental neurocognitive capacity that may contribute to various communication functions and has been found impaired in several developmental disorders. The occurrence of temporal processing dif...

The development of the dental arches in children with oral clefts differs from that in a normal population, due to the type and extension of the cleft, surgical procedure and timing, and decreased growth potential. The size of the maxillary and mandibular dental arches and the amount of interdental space in 3-year-old, cleft-affected and non-cleft children was investigated. Fifty non-cleft (NON...

Median cleft of lower lip and mandible is a rare congenital anomaly described as cleft number 30 of Tessier's classification. In minor forms only lower lip cleft is seen. We report the case of a patient with median cleft of lower lip, severe ankyloglossia, cleft of mandibular symphysis, and residual cleft involving on right soft palate and associated with other facial clefts. These deformities ...