Clinical approach in familial hypophosphatemic rickets: report of three generations
Identifieur interne : 007E46 ( Istex/Corpus ); précédent : 007E45; suivant : 007E47Clinical approach in familial hypophosphatemic rickets: report of three generations
Auteurs : Eduardo Costa Studart Soares ; Fábio Wildson Gurgel Costa ; Thyciana Rodrigues Ribeiro ; Ana Paula Negreiros Nunes Alves ; Cristiane Sá Roriz FontelesSource :
- Special Care in Dentistry [ 0275-1879 ] ; 2013-11.
English descriptors
- KwdEn :
- Abscess, Adult patients, Arabic numerals, Black arrow, Bone loss, Cear, Clinical dentistry, Deciduous, Deciduous dentition, Deciduous teeth, Dental management, Dental treatment, Dentin, Dentistry, Dentition, Differential diagnosis, Dominant trait, Early diagnosis, Early loss, Endod, Familial hypophosphatemic rickets, Federal university, First evidences, Gingival, Histologic, Hypophosphatemic, Hypophosphatemic rickets, Initial presentation, Large pulp chambers, Many teeth, Molar, Multiple tooth loss, Numeral, Oral findings, Oral manifestations, Oral pathol, Oral surg, Panoramic, Panoramic radiography, Pediatric, Pediatric patients, Periodontal, Periodontal disease, Permanent dentitions, Phex gene, Present case report, Proband, Pulp horns, Radiographic, Radiol endod, Rickets, Roman numerals, Spontaneous gingival abscesses, White arrow, Xlhr.
- Teeft :
- Abscess, Adult patients, Arabic numerals, Black arrow, Bone loss, Cear, Clinical dentistry, Deciduous, Deciduous dentition, Deciduous teeth, Dental management, Dental treatment, Dentin, Dentistry, Dentition, Differential diagnosis, Dominant trait, Early diagnosis, Early loss, Endod, Familial hypophosphatemic rickets, Federal university, First evidences, Gingival, Histologic, Hypophosphatemic, Hypophosphatemic rickets, Initial presentation, Large pulp chambers, Many teeth, Molar, Multiple tooth loss, Numeral, Oral findings, Oral manifestations, Oral pathol, Oral surg, Panoramic, Panoramic radiography, Pediatric, Pediatric patients, Periodontal, Periodontal disease, Permanent dentitions, Phex gene, Present case report, Proband, Pulp horns, Radiographic, Radiol endod, Rickets, Roman numerals, Spontaneous gingival abscesses, White arrow, Xlhr.
Abstract
Familial hypophosphatemic rickets is a hereditary disease characterized by the involvement of several family members, transmitted in most cases as an X‐linked dominant trait. Oral manifestations can be the first evidences for an adequate and early diagnosis of X‐linked hypophosphatemic rickets (XLHR). The present report describes the main systemic manifestations, oral findings and dental management in three generations of an affected family. Oral exams, laboratorial and histologic evaluations, cone‐beam computed tomographies, panoramic and periapical radiographs were performed to properly institute the most adequate treatment strategy. The knowledge of clinical signs and symptoms of XLHR is essential for the correct diagnosis of this disease, and for the establishment of preventive and comprehensive dental care.
Url:
DOI: 10.1111/j.1754-4505.2012.00310.x
Links to Exploration step
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<front><div type="abstract">Familial hypophosphatemic rickets is a hereditary disease characterized by the involvement of several family members, transmitted in most cases as an X‐linked dominant trait. Oral manifestations can be the first evidences for an adequate and early diagnosis of X‐linked hypophosphatemic rickets (XLHR). The present report describes the main systemic manifestations, oral findings and dental management in three generations of an affected family. Oral exams, laboratorial and histologic evaluations, cone‐beam computed tomographies, panoramic and periapical radiographs were performed to properly institute the most adequate treatment strategy. The knowledge of clinical signs and symptoms of XLHR is essential for the correct diagnosis of this disease, and for the establishment of preventive and comprehensive dental care.</div>
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<sourceDesc><biblStruct type="case-report"><analytic><title level="a" type="main">Clinical approach in familial hypophosphatemic rickets: report of three generations</title>
<title level="a" type="short">FAMILIAL HYPOPHOSPHATEMIC RICKETS</title>
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