담낭결석이 있는 산모에서 태어난 Binder 증후군 환자 1례
Binder Syndrome Infant Born from Mother with Cholelithiasis
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Binder syndrome is a maxillonasal dysostosis characterized by midface and nasal hypoplasia. It is sometimes associated with short terminal phalanges of fingers and toes and transient radiological features of chondrodysplasia punctata. It is associated with vitamin K deficiency during pregnancy. We describe here a baby with Binder syndrome who was born from mother with cholelithiasis during pregnancy.
Abstract
Binder syndrome is a maxillonasal dysostosis characterized by midface and nasal hypoplasia. It is sometimes associated with short terminal phalanges of fingers and toes and transient radiological features of chondrodysplasia punctata. It is associated with vitamin K deficiency during pregnancy. We describe here a baby with Binder syndrome who was born from mother with cholelithiasis during pregnancy.
참고문헌 (13)
- Noyes F.B., "Case report", Angle Orthod, 9, pp.160~165 (1939)
- Binder K.H., "Dysostosis masillo-nasalis, ein arhinencephaler Missbildungskomplex", Deutsch Zahnaertzl Z, 17, pp.438~444 (1962)
- Sheffield L.J., "Chondrodysplasia punctata-23 cases of a mild and relatively common variety", J Pediatr, 89, pp.916~923 (1976)
- Horswell B.B., "Maxillonasal dysplasia (Binder's syndrome): a critical review and case study", J Oral Maxillofac Surg, 45, pp.114~122 (1987)
- Howe A.M., "The warfarin embryopathy: a rat model showing maxillonasal hypoplasia and other skeletal disturbances", Teratology, 46, pp.379~390 (1992)
- Howe A.M., "Prenatal exposure to phenytoin, facial development, and a possible role for vitamin", K. Am J Med Genet, 58, pp.238~244 (1995)
- Jaillet J., "Biliary lithiasis in early pregnancy and abnormal development of facial and distal limb bones (Binder syndrome): a possible role for vitamin K deficiency", Birth Defects Res A Clin Mol Teratol, 73, pp.188~193 (2005)
- Khau Van Kien P., "Vitamin K deficiency embryopathy", Am J Med Genet, 79, pp.66~68 (1998)
- Sheffield L.J., "Maxillonasal dysplasia (Binder's syndrome) and chodrodysplasia punctata", J Med Genet, 28, pp.503~504 (1991)
- Pauli R.M., "Association of congenital deficiency of multiple vitamin K-dependent coagulation factors and the phenotype of the warfarin embryopathy: clues to the mechanism of teratogenicity of coumarin derivatives", Am J Hum Genet, 41, pp.566~583 (1987)
- Rost S., "Mutations in VKORC1 cause warfarin resistance and multiple coagulation factor deficiency type 2", Nature, 427, pp.537~541 (2004)
- Hunt J.A., "Common craniofacial anomalies: the facial dysostoses", Plast Reconstr Surg, 110, pp.1714~1725 (2002)
- Ferguson J.W., "Maxillonasal dysostosis (Binder syndrome); a review of the literature and case reports", Eur J Orthod, 7, pp.145~148 (1985)
