Modern classification and molecular-genetic aspects of osteogenesis imperfecta.

ABSTRACT: Osteogenesis imperfecta (imperfect osteogenesis in the Russian literature) is the most common hereditary form of bone fragility, it is a genetically and clinically heterogeneous disease with a wide range of clinical severity, often leading to disability from early childhood. It is based on genetic disorders leading to a violation of the structure of bone tissue, which leads to frequent fractures, impaired growth and posture, with the development of characteristic disabling bone deformities and associated problems, including respiratory, neurological, cardiac, renal impairment, hearing loss. Osteogenesis imperfecta occurs in both men and women, the disease is inherited in both autosomal dominant and autosomal recessive types, there are sporadic cases of the disease due to de novo mutations,

SUBMITTER: Zaripova AR 

PROVIDER: S-EPMC7716575 | biostudies-literature | 2020 Mar

REPOSITORIES: biostudies-literature