• Search
  • Advanced Search

Search

  • HOME
  • Search
Case Report
A Case of Tuberculous Osteomyelitis of the Mandible.
T H Son, H K Park, Y S Shin, M J Shin
Clin Exp Pediatr. 1983;26(1):71-75.   Published online January 31, 1983
The predilection sites of skeletal tuberculosis are mainly weight-bearing bones such as vertebrae, hip and knee joint. Involvement of non-weight bearing bones are rare. We experienced an unusual case of tuberculous osteomyelitis of the mandible in 3-year-5-month old female. The diagnosis was established by positive tuberculin skin test, roentgenographic findings and biopsy. Herein, a case of Tuberculous Osteomyelitis of Mandible was presented with...
A Case of Female Pseudohermaphroditism due to Congenital Adrenal Hyperplasia and a Case of Male Pseudohermaphroditism.
Y S Shin, H J Park, H J Chun, M J Shin
Clin Exp Pediatr. 1981;24(12):1203-1208.   Published online December 15, 1981
Recently we experienced each of female and male pseudohermaphroditisms which were admitted with complaint of ambiguous genitalia nearly at thesame time. Case 1, 12 year 7 month old, had musculine appearance with acne, beard and mustache, broad shoulders and short hair. Her phallus was large penile shape with abundant pubic hair and vaginal opening was hidden behind the fused labioscrotal...
Original Article
Clinical Observation of Convulsions in Infancy and Childhood.
H S Jeon, Y S Shin, M J Shin, S C Kang
Clin Exp Pediatr. 1980;23(11):917-926.   Published online November 15, 1980
To assess convulsive disorders in infancy and childhood we have studied clinically about 303 cases who were admitted as convulsions at the Pediatric department of S.R.C.H. from Jun. 1975 to May 1979. These cases were analysed by the route of admission, monthly distribution, age and sex distributions and causes, and also more detailed evaluation for febrile convulsion and epilepsy was...
Case Report
A Case of Prader-Willi Syndrome.
Y M Soung, Y S Shin, M J Shin, S C Kang
Clin Exp Pediatr. 1980;23(7):590-597.   Published online July 15, 1980
Prader-Willi syndrome is characterized by 1) hypotonia in the newborn infant 2) obesity which begins in childhood 3) short stature 4) typical facial features 5) secondary hypogonadism 6) juvenile diabetes mellitus of the maturity-onset type 7) mental retardation The true etiology of Prader-Willi syndrome is still unknown ; however, a hypothalamic disturbance has been postulated. We experienced a 9 year...