KMID : 0361719930040030415
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Korean Journal of perinatology 1993 Volume.4 No. 3 p.415 ~ p.421
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A Case of Sirenomelia
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À¯ÁÖÇö
¹Ú¹®ÀÏ/Á¤¼º·Î/ÀÌÀç¾ï/±è³²ÈÆ/È«Àº°æ
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Abstract
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Sirenomelia is a very rare congenital malformation that has an incidence of 1: 60,000. It is thought to be a sporadic occurrence and nongenetically determined. One of the morphologic characteristics is a fusion of the lower extremity into one
having a
median position. There are varing degrees of severity of the anomalies. We present a case of sirenomelia with review of literature.
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