Transverse facial clefts are rare deformities, these mostly occur as part of syndromes such as facial dysostosis and branchial arch syndrome. This is a report of a case of isolated, asyndromic bilateral facial cleft seen at a semi-urban specialist hospital. Congenital facial defects remain sources of mental and social stress to the families. Infanticide, perhaps a thing of the past in the devel...

BACKGROUND Myotonic Dystrophy Type 1 (DM1) is the most common form of hereditary myopathy presenting in adults. This autosomal-dominant systemic disorder is caused by a CTG repeat, demonstrating various symptoms. A mild, classic and congenital form can be distinguished. Often the quality of life is reduced by orthopaedic problems, such as muscle weakness, contractures, foot or spinal deformitie...

Congenital pseudarthrosis of the tibia continues to pose one of the most difficult problems in paediatric orthopaedic surgery. The surgical procedures most used for treating congenital pseudarthrosis of the tibia are intramedullary nailing associated with bone grafting, vascularized fibular graft and the Ilizarov external circular fixator. Even when union is achieved, the residual deformities i...

IN the early reports on congenital abnormalities in thalidomide babies in Great Britain little attention has been paid to the occurrence of ocular defects. A recent survey by the Chief Medical Officer of the Ministry of Health relating to children born with congenital limb deformities during 1960-62, revealed that there were 652 surviving children with such deformities, 244 of whose mothers had...

introduction: cleft lip and palate is a congenital anomaly occurring in 3 in 1000 live birth. one the major concern in this patient is about cleft gap and its surgical problems. several surgical and non-surgical procedures have been done to decrease this gap. they aimed to achieve the more esthetic results as well as feeding success. nasoalveolar molding (nam) is a new method for reshaping nasa...

Congenital anomalies of the first branchial cleft are rare. Approximately 32 cases of cervicoauricular fistulae have been reported in the past hundred years: this includes the writer's own case in this review. The majority of sinuses and fistulae derived from the lateral cervical vestiges are concerned with the second pharyngeal pouch and its corresponding cleft. Auricular and pre-auricular fis...

A case of a 9-year-old child with hereditary gingival fibromatosis, supernumerary tooth, chest deformities, auricular cartilage deformation, joint laxity and undescended testes is described. The exact mode of inheritance is unclear; a new mutation pattern is possible. These features resemble but differ from the previously reported Laband syndrome. The dental treatment consisted of surgical remo...

Congenital scoliosis is caused by early embryologic errors in vertebral column formation. Defining the deformity, predicting the natural history, and applying the correct treatment can help ensure successful management. Most congenital spine anomalies can be classified, and many have a predictable natural history. Because the deformities are associated with other organ system anomalies in more ...