[Hair collar sign associated with scalp aplasia cutis congenita].
نویسندگان
چکیده
1. Méndez T, Otero I, García R, Pérez B. Síndrome de Klippel-Trenaunay-Weber: presentación de un caso. Rev Cubana Oftalmol. 2001;14:47-9. 2. Bordel MT, Miranda A. Un caso atípico de síndrome de Klippel-Trenaunay. Piel. 2005;20:306-8. 3. Gimeno P, Pérez P, López-Pisón J, Romeo M, Galeano N, Marco M, et al. Síndrome de Klippel-Trenaunay: a propósito de tres nuevas observaciones. An Esp Pediatr. 2000;53:350-4. 4. Lee CW, Choi DY, Oh YG, Yoon HS, Kim JD. An infantile case of SturgeWeber syndrome in association with Klippel-Trenaunay-Weber syndrome and phakomatosis pigmentovascularis. J Korean Med Sci. 2005;20:1082-4. 5. Milhorat TH, Chou MW, Trinidad EM, Kula RW, Mandell M, Wolpert C, et al. Chiari I malformation redefined: clinical and radiographic findings for 364 symptomatic patients. Neurosurgery. 1999;44:1005-17. 6. Elster AD, Chen MY. Chiari I malformations: clinical and radiologic reappraisal. Radiology. 1992;183:347-53. 7. Yancey MK, Lasley D, Richards DS. An unusual neck mass in a fetus with Klippel-Trenaunay-Weber syndrome. J Ultrasound Med. 1993;12:779-82.
منابع مشابه
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ورودعنوان ژورنال:
- Actas dermo-sifiliograficas
دوره 98 6 شماره
صفحات -
تاریخ انتشار 2007