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Cornelia de Lange Syndrome.

Journal of the Korean Pediatric Society 1980;23(6):479-485.
Published online June 15, 1980.
Cornelia de Lange Syndrome.
Hwa Jung Yoon, Ai Lan Kim, Whan Kok Yong, Sung Il Ahn
Department of Pediatrics, Eul Ji General Hospital Seoul, Korea.
Cornelia de Lange 증후군
윤화중, 김애란, 용환극, 안승일
을지병원 소아과
Abstract
The Cornelia de Lange syndrome is characterized by severe growth and mental retardations and a cluster of minor malformations, the facial appearance being most characteristic. In the present paper, we shall report I case of this syndrome in Korean male infant and the variability of de Lange syndrome is discussed. The bady showed hirsutism, low forehead coved with lanugo-like hair, bushy eyebrows that meet in the midline, long curely eyelashes as well as low pitched, growling cry and skeletal abnormalities of hand bones. There is no positive family history and the karyotype was normal. Although the de Lange syndrome has received more interest there is no agreement as to the possible cause.


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