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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Bibliographic Details
Main Authors: И. А. Викторова, Н. В. Коншу, Д. С. Иванова
Format: Article
Language:Russian
Published: SINAPS LLC 2015-04-01
Series:Arhivʺ Vnutrennej Mediciny
Subjects:
Online Access:https://www.medarhive.ru/jour/article/view/391
Description
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.
ISSN:2226-6704
2411-6564