НЕСОВЕРШЕННЫЙ ОСТЕОГЕНЕЗ: ПОЛИМОРФИЗМ КЛИНИЧЕСКИХ ПРОЯВЛЕНИЙ И ТАКТИКА ЛЕЧЕНИЯ
Osteogenesis imperfecta syndrome characterized by clinical manifestations of polymorphism under light for a long time can not be diagnosed, and it becomes apparent only after the symptoms found in children and grandchildren these patients. Management of patients with this nosology requires a multi-c...
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| Main Authors: | , , |
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| Format: | Article |
| Language: | Russian |
| Published: |
SINAPS LLC
2015-04-01
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| Series: | Архивъ внутренней медицины |
| Subjects: | |
| Online Access: | https://www.medarhive.ru/jour/article/view/391 |
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| Summary: | Osteogenesis imperfecta syndrome characterized by clinical manifestations of polymorphism under light for a long time can not be diagnosed, and it becomes apparent only after the symptoms found in children and grandchildren these patients. Management of patients with this nosology requires a multi-component approach in the context of the family with questions of prevention of recurrent fractures, treatment, rehabilitation and disability. |
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| ISSN: | 2226-6704 2411-6564 |