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1.
Article in English | IMSEAR | ID: sea-173940

ABSTRACT

Genetic disorders account for a significant amount of morbidity and mortality in children and are of primary interest to the dentist. Crouzan syndrome is one of a rare group of syndromes characterized by craniosynostosis or premature closing of the cranial sutures. The major features are Brachycephaly, ocular proptosis, under developed maxilla, midface hypoplasia, rare cleft lip, palate. Early Craniectomy is often needed to alleviate the raised intracranial pressure. This paper discusses a case report of five year old girl with the features of crouzan syndrome and a multidisciplinary approach to be followed in managing the situation.

2.
Article in English | IMSEAR | ID: sea-173928

ABSTRACT

Treacher-Collins syndrome (TCS) is a rare congenital, craniofacial disorder that is inherited as an autosomal dominant pattern. The present case report describes TCS in a Caucasian girl aged 8 years with full tetrad of cardinal features in addition to mental retardation, deafness and dumbness since birth. The management of the child while delivering the treatment requires patience, skill and knowledge about the condition, which are essential for a Pedodontist and treatment that has to be tailored to the specific needs of each individual and preferably done by a multidisciplinary management team.

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