2.Untreated Congenital Vertical Talus Associated with Tarsal Codlition: A Case Report
Chang Gon KIM ; Sang Wan LEE ; Byung Duk PARK
The Journal of the Korean Orthopaedic Association 1971;6(2):139-142
Congenital vertical talus associating tarsal coalition, which is a very anomalous condition and causes severe rigid flat foot, is presented with literary reviews. This case was treated with soft tissue release and triple arthrodesis.
Arthrodesis
;
Flatfoot
;
Talus
3.Correction of the ear lobe defect.
Chang Gon KWAK ; Chung Hyun CHANG ; Won Yong YANG ; Doo Hyung LEE
Journal of the Korean Society of Plastic and Reconstructive Surgeons 1992;19(4):647-655
No abstract available.
Ear*
4.Anatomic Aspects of Intermittent Exotropia in Childhood.
Journal of the Korean Ophthalmological Society 2001;42(10):1440-1444
PURPOSE: This study aimed to find out the difference in between the anatomic properties children with intermittent exotropia and children with orthophoria. METHODS: The intermittent exotropia group consisted of 35 patients who had an angle of deviation of more than 15 prisms. The control group consisted of 35 orthophoric children with comparable age and sex ratio. From the view of skull AP, we compared the diameter, interlateral wall distance, and intermedial wall distance of the orbital rim. Also we compared the intercanthal distance, interlateral canthal distance of eyelids, and interpupillary distance. RESULTS: The average values of interpupillary distance, intercanthal distance, and interlateral canthal distance of exotropic group were 54.23+/-1.85 mm, 34.75+/-1.66 mm, and 78.25+/-4.21 mm, respectively. Compared to those of control group, which were 53.59+/-1.21 mm, 33.56+/-1.54 mm, and 76.68+/-3.23 mm, respectively, there was no significant difference (P>0.05). The average values of the diameter, interlateral wall distance and the intermedial wall distance of the orbital rim were not significantly different between two groups (p>0.05). CONCLUSIONS: Our results showed that the anatomic properties including orbital rim size and orbital exodeviation did not seen to influence the development of intermittent exotropia.
Child
;
Exotropia*
;
Eyelids
;
Humans
;
Orbit
;
Sex Ratio
;
Skull
5.A Case of Amyopathic Dermatomyositis.
Korean Journal of Dermatology 2001;39(7):827-828
Amyopathic dermatomyositis is diagnosed when the biopsy-confirmed cutaneous lesions of dermatomyositis are present for longer than 2 years in the absence of muscle weakness, elevated muscle enzymes, and the history of immunosuppressive drug therapy and ingestion of drugs such as hydroxyurea that can produce dermatomyositis-like cutaneous hypersensitivity changes. We report a 36-year-old woman with a 3-year history of typical skin features of dermatomyositis with no evidences of muscle involvement.
Adult
;
Dermatomyositis*
;
Drug Therapy
;
Eating
;
Female
;
Humans
;
Hydroxyurea
;
Hypersensitivity
;
Muscle Weakness
;
Skin
6.Comparision of the Two Groups between Autologous Bone Chips and Cage as Posterior Lumbar Interbody Fusion in Spondylolisthesis Patients.
Pill Jae SHIN ; Chang Hyun KIM ; Jae Gon MOON ; Ho Kook LEE ; Do Yun HWANG
Journal of Korean Neurosurgical Society 2000;29(4):507-513
No abstract available.
Humans
;
Spondylolisthesis*
9.A Case of Congenital Leukemia Cutis.
Young Suck RO ; Deug Gon MOON ; Chang Woo LEE ; Haeng Gon HAN ; Hahng LEE ; Jae Kyung CHOI
Korean Journal of Dermatology 2000;38(8):1089-1093
Congenital leukemia is a rare disease developing within the first 4 to 6 weeks of life, whose natural history is quite different from that of childhood and adult leukemia. Leukemia cutis occurs in 25% to 30% of infants with congenital leukemia and is more frequently associated with acute myeloid leukemia than acute lymphocytic leukemia. We report a case of congenital leukemia cutis in which a walnut-sized, slightly erythematous, dome-shaped tumor that had developed at left frontal area since birth was confirmed by skin biopsy. A review and analysis of Korean literature pertaining specially to leukemia cutis in congenital leukemia is presented along with the report of an additional case.
Adult
;
Biopsy
;
Humans
;
Infant
;
Leukemia*
;
Leukemia, Myeloid, Acute
;
Natural History
;
Parturition
;
Precursor Cell Lymphoblastic Leukemia-Lymphoma
;
Rare Diseases
;
Skin
10.Case reports of bone grafting in unilateral alveolar-palatal cleft patients.
Yun Ho BAE ; Jae Hyun PARK ; Myeong Jin LEE ; Chang Gon LEE ; Byung Rho CHIN ; Hee Kyeung LEE
Yeungnam University Journal of Medicine 1991;8(1):198-205
We obtained successful functional and esthetic results by grafting of iliac marrow-cancellous bone in 2 cases of alveolar-palatal cleft patients. Bone graft of alveolar-palatal clefts provide bony support to adjacent teeth of cleft area, prevented from relapse of orthodontic arch expansion, closure of oroantral fistula and improvement of speech problem. 1. In one case, extraction of upper right central incisor that was little bone support, alignment of rotated teeth and expansion of collapsed arch segment were done with pre-orthodontic treatment. The other case. Bone grafting was done after removal of prosthesis with no pre-orthodontic treatment. 2. After mucoperiosteal incision in cleft area, the mucosal flap of labial area, palate and nose were separation and the raised nasal mucosa was sutured for closure of oroantral fistula. Then, the iliac marrow-cancellous bones were grafted to cleft site. 3. After 6 months of operation, we had seen the new bone deposition to cleft site in dental radiograph and prosthetic treatment of missing teeth were done.
Bone Transplantation*
;
Humans
;
Incisor
;
Nasal Mucosa
;
Nose
;
Oroantral Fistula
;
Palate
;
Prostheses and Implants
;
Recurrence
;
Tooth
;
Transplants