Download A color atlas of orofacial health and disease in children by Crispian Scully, Richard Welbury, Catherine Flaitz, Oslei PDF

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By Crispian Scully, Richard Welbury, Catherine Flaitz, Oslei Paes de Almeida

Like the profitable first version, this stronger, up to date and extended moment variation profiles the typical orofacial issues and a variety of much less universal and a few infrequent problems. the focal point is at the incidence of those issues in kids and youth, and the writer tailors the remark to express pediatric age teams. within the new version, the textual content comprises remedy strategies for the commonest oral illnesses. Any health care professional referred to as upon to diagnose and deal with youngsters who've orofacial difficulties will enjoy the wealth of fabric provided here.

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Extra resources for A color atlas of orofacial health and disease in children and adolescents: diagnosis and management

Example text

Apert’s syndrome (Figs 99, 100) also involves progressive synostosis of bones in the hands, feet and vertebrae as well as ankylosis of joints. Palatal anomalies are common in Apert’s syndrome, and one-third of patients have cleft palate. Maxillary hypoplasia is also seen. Crouzon’s syndrome is discussed on p. 49. Diagnosis Diagnosis is clinical, supported by imaging. Management Medical care is usually required and craniofacial surgery and genetic counseling may be indicated. 100 Figure 100. Digital anomalies in Apert’s syndrome.

Apert’s syndrome (Figs 99, 100) also involves progressive synostosis of bones in the hands, feet and vertebrae as well as ankylosis of joints. Palatal anomalies are common in Apert’s syndrome, and one-third of patients have cleft palate. Maxillary hypoplasia is also seen. Crouzon’s syndrome is discussed on p. 49. Diagnosis Diagnosis is clinical, supported by imaging. Management Medical care is usually required and craniofacial surgery and genetic counseling may be indicated. 100 Figure 100. Digital anomalies in Apert’s syndrome.

44 Figure 44. 5 years. There has been loss of enamel from the primary incisors, canines and first molars. Periapical radiolucencies are not uncommon. • Type II (hereditary opalescent dentine). • Type III (Brandywine type). This extreme variation is recognized in the primary dentition where the teeth have a ‘shell-tooth’ appearance and multiple pulpal exposures are common. Diagnosis Diagnosis is clinical, supported by imaging. Management Restorative dentistry is usually indicated and genetic counseling.

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