Oral and craniofacial manifestations in a Hunter syndrome patient with hematopoietic stem cell transplantation: A case report
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- Rafaela de Oliveira Torres
- Department of Pediatric Dentistry and Orthodontics Universidade Federal do Rio de Janeiro Brazil
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- Andréa Vaz Braga Pintor
- Department of Pediatric Dentistry and Orthodontics Universidade Federal do Rio de Janeiro Brazil
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- Fábio Ribeiro Guedes
- Department of Oral Pathology Universidade Federal do Rio de Janeiro Brazil
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- Liana Bastos Freitas‐Fernandes
- Department of Pediatric Dentistry and Orthodontics Universidade Federal do Rio de Janeiro Brazil
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- Anneliese Lopes Barth
- Department of Genetics Instituto Fernandes Figueira Brazil
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- Dafne Dain Gandelman Horovitz
- Department of Genetics Instituto Fernandes Figueira Brazil
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- Ivete Pomarico Ribeiro de Souza
- Department of Pediatric Dentistry and Orthodontics Universidade Federal do Rio de Janeiro Brazil
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説明
<jats:title>ABSTRACT</jats:title><jats:p>We described herein the oral and craniofacial features of a 7‐year‐old boy, diagnosed <jats:italic>in utero</jats:italic> with mucopolysaccharidosis II (MPS II), who was treated with hematopoietic stem cell transplantation (HSCT) at 70 days of age. The main oral clinical findings were the following: macroglossia, posterior cross‐bite, crowding, pointed cuspid teeth, delayed tooth eruption, retained primary teeth, and enamel hypoplasia. The image examination showed: retention eruption, posterior primary teeth with short roots, absence of some permanent teeth, and stretching of the stylohyoid processes bilaterally. This patient showed the importance of early diagnosis and HSCT therapy in attenuating the clinical and radiographic oral and craniofacial manifestations of the MPS II patient.</jats:p>
収録刊行物
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- Special Care in Dentistry
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Special Care in Dentistry 38 (1), 51-54, 2018-01
Wiley
