- Original Article
- a case of type II lissencephaly; Walker-Earburg syndrome.
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Ae Yong Kim, Jung Ho Lee, Yong Sub Kim, Kyeng Sook Cho, Jong Dai Jo
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Clin Exp Pediatr. 1991;34(11):1598-1604. Published online November 30, 1991
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Lissencephaly is a rare abnormality of brain development characterized by incomplete neuronal
migration and a smooth cerebral surface. Three types of lissencephaly are recognized. Type I is
characterized by microcephaly and dysmorphic facies. Type II usually lacks characteristic facies but
exhibits macrocephaly from hydrocephalus, eye anomaly, and/or congenital muscular dystrophies.
Type III is characterized by microcephaly without any characteristic dysmorphic facial features.
We have experienced... |
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- A Case of Arthrogryposis Multiplex Congenita in Identical Twin.
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Chang Il An, Byeong Gu Min, Kyeng Sook Cho, Jong Dai Jo
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Clin Exp Pediatr. 1990;33(10):1429-1433. Published online October 31, 1990
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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. |
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- A Case of Acute Lymphocytic leukemia in a Newborn.
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Young Jin Min, Myoung Hee Cha, Kyeng Sook Cho, Jong Dai Jo
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Clin Exp Pediatr. 1988;31(9):1197-1201. Published online September 30, 1988
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The case of a 13 day-old baby is reported who satisfied the usual diagnostic criteria for congenital
leukemia. |
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