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Case Report

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 the Dubowitz Syndrome.

Kyung Ae Lee, Chi Ho Yun, Jae Sun Jung, Hee Ju Kim, Sung Ill Ahn, Hyung Ro Moon

Clin Exp Pediatr. 1986;29(4):436-440. Published online April 30, 1986

The Dubowitz syndrome is an autosomal recessive condition characterized by intrauterine growth retardation, postnanal growth retardation, peculiar facial appearance, short stature, low birth weight, microcephaly and borderline intelligence or mild mental retardation. We reported a typical case of the Dubowitz syndrome in a full term male infant together with a brief review of pertinent literatures since the incidence of the...

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