Add to ORKGOsteogenesis imperfecta is an inherited disorder of the connective tissue. The extreme bone fragility seen in patients suffering from osteogenesis imperfecta pose a series of problems with regard to behavior management and rendering of quality dental treatment. Presented here a case of a four year old child suffering from osteogenesis imperfecta
Background. Osteogenesis imperfecta (OI), also known as ""brittle bone disease,"" can be difficult t...
Dental development is part of the craniofacial organogenesis, starting from the pluripotent cephalic...
Osteogenesis imperfecta (OI) is a rare hereditary condition caused by changes in collagen metabolism...
Osteogenesis imperfecta (OI), an inherited skeletal disorder characterized by low bone mass, bone fr...
Osteogenesis imperfecta is one of the most commonly recognized inheritable disorders of the connecti...
Osteogenesis imperfecta (OI) is a rare hereditary disease caused by mutations in genes coding for ty...
Osteogenesis imperfecta (OI) is a rare disease with a wide spectrum of clinical and genetic variabil...
Osteogenesis imperfecta is a heritable disorder of connective tissue, affecting both bone and soft t...
The authors present a case of Osteogenesis Imperfecta, emphasizing the clinical and epidemiological ...
This paper presents a review of dentinogenesis imperfecta occurring in patients with osteogenesis im...
Osteogenesis imperfecta is a syndrome of interest to dentists because dentinogenesis imperfecta is f...
Osteogenesis imperfecta (OI) is a genetic disorder that is usually caused by disturbed production of...
Osteogenesis imperfecta (OI), a secondary cause of osteoporosis, principally manifests as bone fragi...
Osteogenesis imperfecta (OI) is the most frequent hereditary bone disease during childhood. In most ...
Osteogenesis imperfecta is a hereditary connective tissue disorder characterized primarily by fractu...
Background. Osteogenesis imperfecta (OI), also known as ""brittle bone disease,"" can be difficult t...
Dental development is part of the craniofacial organogenesis, starting from the pluripotent cephalic...
Osteogenesis imperfecta (OI) is a rare hereditary condition caused by changes in collagen metabolism...
Osteogenesis imperfecta (OI), an inherited skeletal disorder characterized by low bone mass, bone fr...
Osteogenesis imperfecta is one of the most commonly recognized inheritable disorders of the connecti...
Osteogenesis imperfecta (OI) is a rare hereditary disease caused by mutations in genes coding for ty...
Osteogenesis imperfecta (OI) is a rare disease with a wide spectrum of clinical and genetic variabil...
Osteogenesis imperfecta is a heritable disorder of connective tissue, affecting both bone and soft t...
The authors present a case of Osteogenesis Imperfecta, emphasizing the clinical and epidemiological ...
This paper presents a review of dentinogenesis imperfecta occurring in patients with osteogenesis im...
Osteogenesis imperfecta is a syndrome of interest to dentists because dentinogenesis imperfecta is f...
Osteogenesis imperfecta (OI) is a genetic disorder that is usually caused by disturbed production of...
Osteogenesis imperfecta (OI), a secondary cause of osteoporosis, principally manifests as bone fragi...
Osteogenesis imperfecta (OI) is the most frequent hereditary bone disease during childhood. In most ...
Osteogenesis imperfecta is a hereditary connective tissue disorder characterized primarily by fractu...
Background. Osteogenesis imperfecta (OI), also known as ""brittle bone disease,"" can be difficult t...
Dental development is part of the craniofacial organogenesis, starting from the pluripotent cephalic...
Osteogenesis imperfecta (OI) is a rare hereditary condition caused by changes in collagen metabolism...