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KMID : 0358419920350091396
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Korean Journal of Obstetrics and Gynecology
1992 Volume.35 No. 9 p.1396 ~ p.1400
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Achondrogenesis Type I - A Case Report -
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김세광/Kim SK
이보연/박용원/조재성/양영호/송찬호/Lee BY/Park YW/Cho JS/Yang YH/Song CH
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Abstract
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Achondrogenesis is a rare lethal form of congenital micromelic dwarfism in which there is a defect in enchondral ossification. A 22-year-old multiparous woman was referred to our hospital at 19 weeks gestation because of a malformed fetus. An ultrasound examination showed fetal hydrops, omphalocele, and extremely short extremities. The pregnancy was terminated with the delivery of a grossly malformed stillborn male fetus. Radiololgical and pathological examination of the fetus confirmed the diagnosis of achondrogenesis type I.
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