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Case Report
A Case of ARCI Syndrome with Hypoplasia of Corpus Callosum and Heart Anomaly
Eo-Jin Kim, Young-Ran Yoon, Min-Hae Lee, Ki-Su Kang, Jae-Young Lim, Myoung-Bum Choi, Chan-Hoo Park, Hyang-Ok Woo, Hee-Shang Youn
Clin Exp Pediatr. 2003;46(8):826-830.   Published online August 15, 2003
ARCI syndrome consists of arthrogryposis, renal tubular acidosis, cholestatic jaundice and icthyosis. We experienced an ARCI syndrome case with corpus callosum hypoplasia and atrial septal defect. This case had oral feeding difficulty, multiple joint contracture, renal tubular acidosis and neurogenic muscular atrophy at neonatal period. At two months of age, icthyosis and cholestatic jaundice were diagnosed. The case was hospitalized...
A Case of Neonatal Cholestasis with Arthrogryposis Multiplex Congenita and Renal Tubular Insufficiency(ARC Syndrome)
Hi Soo Rhee, Soon Young Kim, Nam Sun Baik, Il Soo Ha, Jeong Kee Seo
Clin Exp Pediatr. 1996;39(1):126-130.   Published online January 15, 1996
We report a case of ARC syndrome with arthrogryposis multiplex congenita, renal tubular insufficiency and cholestasis. The Patient presented in the early neonatal period with micrognathia, low set ears, high arched palate, multiple joint contracture, conjugated hyperbilirubinemia and failure to thrive. He died at the age of 1 month despite medical therapy. Findings of renal tubular insufficiency included persistent renal...
A Case of Arthrogryposis Multiplex Congenita with Congenital Hypertropic Pyloric Stenosis
Seung Chul Yang, So Young Kim, Hyun Hi Kim, Seung Hoon Han, Jong In Byun, Won Bae Lee
Clin Exp Pediatr. 1995;38(11):1577-1582.   Published online November 15, 1995
Arthrogryposis multiplex congenita is a congenital syndrome characterized by extreme stiffness and contracture of multiple joints and associated hypoplasia or absence of development of muscle, bone, and soft tissues; and refers to a heterogeneous group of congenital disorders of unknown but probably multiple etiologies. We present a 50 days old male baby who has had mmultiple fixed contractures of joints...
Arthrogryposis Multiplex Congenita in Siblings
Kyoung Hee Choi, Jeong Ah Park, Kyoung Sim Kim, Ki Bok Kim
Clin Exp Pediatr. 1995;38(9):1293-1298.   Published online September 15, 1995
Arthrogryposis multiplex congenita is a rare congenital disorder characterized by multiple fixed-joint deformities of the upper and lower extremities. Most cases are sporadic, although rare cases of familial recurrence are reported worldwide. Recently, we experienced 2 cases of arthrogryposis multiplex congenita in a family (a brother and a sister). They were born with micrognathia, low set ears, broad and short...
A Case of Arthrogryposis Multiplex Congenita
Jong Min Lee, Su Min Kim, Hyung Kun Nam, Jin Sam No
Clin Exp Pediatr. 1992;35(6):834-839.   Published online June 15, 1992
The simple definition of arthrogryposis is "a syndrome of persistent joint contractures present at birth" We have experienced a 4 days-old male baby who had multiple joint contractures with muslce atrophy. Diagnosis was arthrogryposis multiplex congenita and made by clinical finding. A brief review of the literature was made.
Original Article
A Case of Arthrogryposis Multiplex Congenita in Identical Twin.
Chang Il An, Byeong Gu Min, Kyeng Sook Cho, Jong Dai Jo
Clin Exp Pediatr. 1990;33(10):1429-1433.   Published online October 31, 1990
Arthrogryposis Multiplex Congenita is a very rare disease of persistent joint abnormalities present at birth. We experienced a case of arthrogryposis multiplex congenita in identical twin, and a review of literature was made.
Case Report
A Case of Arthrogryposis Multiplex Congenita.
S S Kee, S K Hwang, B I Choo, H G Yun, H S Lee, S J Oh
Clin Exp Pediatr. 1986;29(3):322-326.   Published online March 31, 1986
A case of Arthrogryposis in 8 days old male baby is reported in Incheon Gill Hospital. This patient was admitted with chief complaints of multiple joint contracture and respiratory disturbance and was expired due to sepsis and respiratory infection. The diagnosis was made by clinical finding, and histologic finding. Histologic findings were reported degeneration of the anterior horn cell of the spinal...
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