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Original Article
Two Cases of Osteogenesis Imperfecta Congenita.
Soon Soen Lim, Byeung Ho Lee, Young Ha Kim, Moon Ki Joe
Clin Exp Pediatr. 1988;31(8):1085-1090.   Published online August 31, 1988
Osteogenesis imperfecta is an inherited disorder of connective tissue that affects the skeleton, ligament, skin, sclerae and dentin. It is thought to be characterized by the abnormal maturation of collagen in both mineralized and nonmineralized tissues. The three major clinical criteria are osteoporosis with abnormal fragility of the skeleton, blue sclerae and dentinogenesis imperfecta. The presence of two of these abnormalities confirms the diagnosis. We have...
Case Report
A case of Congenital Osteogenesis Imperfecta.
Suck Young Lee, Yoon Ho Kang, Sang Keun Oh, Mi Sook Park, Hee Dae Park, Dong Hwan Cha
Clin Exp Pediatr. 1986;29(5):575-578.   Published online May 31, 1986
The authors experienced a case of osteogenesis imperfecta in a 1 st day of life male patient. Characteristic findings of this disease are spontaneous fractures of bones, hypermobility of joints, otosclerosis, deafness and blue sclera. Diagnosis was confirmed by clinical symptoms and radiologic findings. Related literature was briefly reviewed.
A Case of Osteogenesis Imperfecta.
Kwang Wook An, Chull Zoo Jung, Hyo Seop Joo, Seung Woo Moon
Clin Exp Pediatr. 1986;29(1):84-87.   Published online January 31, 1986
Osteogenesis imperfecta is an inherited disorders of connective tissue that affects the skeleton, ligament, sclera, and dentin. Characterized clinical manifestation are multiplefracture, blue sclera, deafness, joint laxity, thin skin, and odontogenesis imperfecta. We experienced acase of osteogenesis imperfecta in a one day old male newborn who chiefly complain respiratory distress, triangular shaped head and fracture and deformity of lower extremity....
A Case of Osteogenesis Imperfecta.
Sang Wook Song, Hu Seok Jung, Kyung Tae Kim, Jung Hee Lee
Clin Exp Pediatr. 1985;28(1):90-94.   Published online January 31, 1985
Osteogenesis imperfecta is an inherited disorder of connective tissue that affects the skeleton, ligaments, skin, sclera and dentin. We experienced a 2 month old female infant of osteogenesis imperfecta. The present case showed failure to thrive, multiple fracture of the bone, thinning of cortex, osteoporosis, blue sclera, high-arched palate and craniotabes. For the treatment of the fracture of right femur,...
A Case of Osteogenesis Imperfecta Type II.
Chang Ick Lee, Young Ai Kim, Jung Joo Kim, Dong Hak Shin
Clin Exp Pediatr. 1984;27(1):93-97.   Published online January 31, 1984
Osteogenesis, imperfecta is an inherited disorder of connective tissue characterized by multiple fractures, blue sclerae, progressive deafness, loose jointedness, and skin. We experienced a case of Type I osteogenesis imperfecta in a 2 months old male infant who visited our hospital with chief complaints of generalized growth retardation, blue sclera and frequent fractures and deformities of limbs. With typical manifestation...
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