Type I osteogenesis imperfecta: a case report

The term osteogenesis imperfecta includes several genetic defects of type I collagen, clinically traduced in bone fragility and deformity. The type I or Lobstein variety is the most frequent form of the disease and is characterized by a pattern of autosomal dominant inheritance. The case of a 65-ye...

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Bibliographic Details
Main Authors: David Armando Guach Hevia, Carlos Rafael Almira Gómez
Format: Article
Language:English
Published: Universidad de Ciencias Médicas de Holguín 2022-02-01
Series:Correo Científico Médico
Online Access:https://revcocmed.sld.cu/index.php/cocmed/article/view/3955
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