- Case Report
- The May-Hegglin Anomaly in a Family
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Jin Ho Lee, Su Yeon Park, Yong Sub Kim, Jong Dai Jo, Byung Chang Kim
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Clin Exp Pediatr. 1994;37(10):1449-1452. Published online October 15, 1994
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The May-Hegglin anomaly is a rare autosomal dominant trait characterized by platelet abnormalities in the peripheral blood and large(up to 5μ) pale blue staining inclusionsl in the cytoplasm of neutrophils, eosinophils, basophils, and
We experienced a case of May-Hegglin anomaly in a 7 year old male and another case out of his family. His initial complaints at the admission were... |
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- 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 the Membranous Type of Prepyloric Gastric Atresia.
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Young Soon Shin, Byeng Gu Min, Kyeong Sook Cho, Jong Dai Jo
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Clin Exp Pediatr. 1990;33(9):1276-1280. Published online September 30, 1990
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Gastric atresia is a very rare congenital anomaly that causes obstructive symptoms.
In 1965 Gerber classified this anomaly.
According to this classification, we recently experienced a case of the membranous type of
prepyloric gastric atresia in a 30 month old female, diagnosed by clinical, radiological, and surgical
findings.
And we report this case with a review of literature. |
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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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