A Case of Perinatal Lethal Osteogeenesis Imperfecta / 대한주산의학회잡지
Korean Journal of Perinatology
; : 55-59, 1997.
Article
in Ko
| WPRIM
| ID: wpr-100469
Responsible library:
WPRO
ABSTRACT
Osteogenesis imperfecta is a rare congenital disease. It is a heterogeneous group of inherited disorders characterized by multiple bone fracture, blue sclera, hearing loss, abnormalities of dentition and widespread connective tissue ahnormality. We experienced a case of osteogenesis imperfecta diagnosed in utero by ultrasonogram and confirmed hy postnatal radiograph after delivery. We present the case with a hrief review of the literature.
Key words
Full text:
1
Index:
WPRIM
Main subject:
Osteogenesis Imperfecta
/
Sclera
/
Ultrasonography
/
Connective Tissue
/
Dentition
/
Fractures, Bone
/
Hearing Loss
Type of study:
Diagnostic_studies
Language:
Ko
Journal:
Korean Journal of Perinatology
Year:
1997
Type:
Article