Biótipo da criança com osteogênese imperfeita
This work was developed by an OI referencial center, involving studies of pacients during the treatment between 1995 and 2005. Fifteen pacients´ records were selected, the average of their age was 8,2 years old. As a result, we got eleven females and four males, six of them held the type I of OI;...
| Main Authors: | , , |
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| Format: | Article |
| Language: | Portuguese |
| Published: |
Universidade Nove de Julho
2008-01-01
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| Series: | ConScientiae Saúde |
| Online Access: | http://www.redalyc.org/articulo.oa?id=92970117 |
| Summary: | This work was developed by an OI referencial center, involving studies of pacients
during the treatment between 1995 and 2005. Fifteen pacients´ records
were selected, the average of their age was 8,2 years old. As a result, we got eleven
females and four males, six of them held the type I of OI; five, the type III; and
four, types IV. In seven cases the broken bones occurrence was higher with the
three-year-old children. Cases of OI ancestors were found in different levels of
kinship: six of them could walk and nine had difficulty walking or simply could
not. Regarding the deformities, 13 of them had bluish sclera; nine, dentinogenesis
imperfecta; one, visual accuracy problems; and five had no deformities. |
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| ISSN: | 1677-1028 1983-9324 |