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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 Fanconi's Anemia.
Dong Hwan Cha, Jung Shim Choi, Kwang Ho Kim, Hong Ku Lee, Sha Sook Hahn
Clin Exp Pediatr. 1983;26(8):808-811.   Published online August 31, 1983
Recently we experienced a case of Fanconist anemia in a 6 years old male child and reported with brief reviews of literatures. The initial symptom was nasal bleeding and pallor which observed between age of 4 years to 6 years. He was microcephaly, His both thumbs were rudimentary. Cystogenic study showed chromosomal breakage. Bone marrow study showed hypocellularity.
A Case of Weismann-Netter Stuhl Syndrome.
Kwang Ho Kim, Hong Ku Lee, Dong Hwan Cha, Jung Sim Choi, Chie Ja Cho, Jung Sook Lee
Clin Exp Pediatr. 1983;26(6):622-625.   Published online June 30, 1983
Weismann-Netter-Stuhl syndrome is congenital anterior bowing of the diaphyses of the tibia and fibula usually bilateral and symmetical, which is clinically resembles the sabre shin of syphilis. A case of Weismann-Netter-Stuhl syndrome in a 5 years oldboy was presented with a brief review of literature. This boy showed stunted growth, anterior bowing of legs and moderate degree of dyphosis, clear intelligence. X-ray showed...
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