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 ...

Cleft lip and cleft palate has got a high incidence in Asian births. There are different techniques for closure of the cleft. The furlows double opposing Z-plasty repair of cleft palate was first described by Leonard Furlow in 1978. Here we present 2 case of cleft palate treated with Furlows double opposing Zplasty.

basal encephalocele is a rare craniofacial anomaly. in the present paper we report a 10-year-old boy presented with cleft palate, congenital nystagmus, and hypertelorism. during preoperative evaluation for cleft palate repair, a pulsatile mass was detected in the pharynx. magnetic resonance imaging showed sphenoethmoidal type of basal encephalocele and agenesis of corpus callosum. neurosurgical...

We present an epidemiologic study of cleft lip and palate in the Republic of Korea from January 1, 1993 through December 31, 1993. In 1993, the number of total live births was 715,817. And from 1993 through 1995, a total of 1,293 new patients with cleft lip and palate who were born in 1993 were identified. The incidence of cleft lip and palate was 1.81 per 1000, that is, 1 per 554 live births. ...

Children born with a cleft lip and or palate face numerous difficulties during the course of their lives. Their families must respond to the challenge of a high level of burden of care required by these patients. The studies listed in this thesis benchmark the characteristics of cleft lip and palate in a cohort of patients living in Northern Finland. These studies strived to consider epidemiolo...

patients and methods the study population comprised 20 children with cleft palate, six to nine years old, after first surgery, with normal intelligence, and 40 normal children with normal iq levels and no speech-language disorders. in this cross-sectional study, oral stereognosis was investigated by identification of objects with different shapes and surface alterations, when placed in the mout...

BACKGROUND There are many countries in the world where patients with cleft lip and palate cannot get access to specialized cleft care units. Cleft missions play an important role in providing surgical care to the areas of the world with limited resources. This article presents a model of cleft missions that can be adopted in many countries where expertise is available but resources are limited....