INTRODUCTION: Osteogenesis imperfecta (OI) is a rare, inherited systemic connective tissue disease that causes decreased bioavailability of collagen type 1. Collagen type 1 is the most abundant connective tissue in the body and a key part of many organs. While the bone phenotype in OI is well described, less is known about the effects of decreased collagen on other organs. In the heart, collagen type 1 is present in the heart valves, chordae tendineae, annuli fibrosi and the interventricular septum. It is thus likely that the heart is affected in OI.OBJECTIVES: The aim of this systematic literature review was to investigate whether patients with OI have an increased risk of cardiovascular disease compared to healthy adults.DATA SOURCES: Pub...
AbstractBackgroundOsteogenesis imperfecta is a genetic disorder of bones, which has different types....
Osteogenesis imperfecta (OI) is an inherited connective tissue disorder with skeletal dysplasia of v...
Purpose: Osteogenesis imperfecta (OI) is a rare inherited heterogeneous connective tissue disorder c...
AbstractBackgroundOsteogenesis imperfecta (OI) is a hereditary connective tissue disease often due t...
Osteogenesis imperfecta (OI) type I is a hereditary disorder of connective tissue (HDCT) characteriz...
Osteogenesis imperfecta (OI) type I is a hereditary disorder of connective tissue (HDCT) characteriz...
Osteogenesis imperfecta (OI) is a rare inherited connective disorder causing increased bone fragilit...
Objective: Osteogenesis imperfect (OI) is an inherited disorder of type1 collagen synthesis with var...
To investigate the prevalence of cardiac abnormalities in osteogenesis imperfecta we performed a cli...
Osteogenesis imperfecta (OI) is a hereditary connective tissue disorder, usually caused by dominant ...
Article; Early AccessObjectives: Osteogenesis imperfecta (OI) is a disease caused by defective colla...
We report a patient with severe aortic and mitral regurgi-tation secondary to osteogenesis imperfect...
Osteogenesis imperfecta (OI) is a connective tissue disorder that is caused by genetic mutation. OI ...
Background: Osteogenesis imperfecta is a genetic disorder of bones, which has different types. Type ...
ABSTRACT While aortic root dilatation and valvular dysfunction have been well-documented in osteogen...
AbstractBackgroundOsteogenesis imperfecta is a genetic disorder of bones, which has different types....
Osteogenesis imperfecta (OI) is an inherited connective tissue disorder with skeletal dysplasia of v...
Purpose: Osteogenesis imperfecta (OI) is a rare inherited heterogeneous connective tissue disorder c...
AbstractBackgroundOsteogenesis imperfecta (OI) is a hereditary connective tissue disease often due t...
Osteogenesis imperfecta (OI) type I is a hereditary disorder of connective tissue (HDCT) characteriz...
Osteogenesis imperfecta (OI) type I is a hereditary disorder of connective tissue (HDCT) characteriz...
Osteogenesis imperfecta (OI) is a rare inherited connective disorder causing increased bone fragilit...
Objective: Osteogenesis imperfect (OI) is an inherited disorder of type1 collagen synthesis with var...
To investigate the prevalence of cardiac abnormalities in osteogenesis imperfecta we performed a cli...
Osteogenesis imperfecta (OI) is a hereditary connective tissue disorder, usually caused by dominant ...
Article; Early AccessObjectives: Osteogenesis imperfecta (OI) is a disease caused by defective colla...
We report a patient with severe aortic and mitral regurgi-tation secondary to osteogenesis imperfect...
Osteogenesis imperfecta (OI) is a connective tissue disorder that is caused by genetic mutation. OI ...
Background: Osteogenesis imperfecta is a genetic disorder of bones, which has different types. Type ...
ABSTRACT While aortic root dilatation and valvular dysfunction have been well-documented in osteogen...
AbstractBackgroundOsteogenesis imperfecta is a genetic disorder of bones, which has different types....
Osteogenesis imperfecta (OI) is an inherited connective tissue disorder with skeletal dysplasia of v...
Purpose: Osteogenesis imperfecta (OI) is a rare inherited heterogeneous connective tissue disorder c...