ALBINISMO PARCIAL: REPORTE DE TRES CASOS

REFERENCIAS BIBLIOGRÁFICAS

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2. Genetic Skin disorders. Albinism with deafness pg 318-333.

3. BALDWIN CT, HOTH CF, MACINE RA, MILUNSKY A. Mutations in PAX3 that cause waardenburg syndrome type 1: ten new mutations and review of the literature. Am J Med Genet 1995; 58:115-22.

4. BROWN KS, BERGSMA DR, BARROW MV. Animal models of pigment and hearing abnormalities in man . Birth Defects 1971;102-9.

5. SHAH KN, DALAL SJ, DESAI MP, SHETH PN, et al. White forelock, pigmentary disorder of irides and long segment Hirschsprung disease: possiblevariant of Waardenburg syndrome. J Pediatr 1981;99:432-5. 

6. TASSABEHJI M, NEWTON VE, LIU XZ, BRADY, A, DONNAI D, KRAJEWSKA-WALASEK M, et al. The mutational spectrum in Waardenburg syndrome. Hum Molec Genet 1995;4;2131-7.

7. EZOE K, HOLMES SA, Ho L. Novel mutations and deletions of the KIT (steel factor receptor) gene in human piebaldism. Am J Hum Genet 1995 Jan ;56(1):58-66

8. RICHARDS KA, FUKAI K, OISO N. A novel KIT mutation results in piebaldism with progressive depigmentation J. Am Acad Dermatol 2001;44(2):288-92.

9. SPRITZ RA. Piebaldism, Waardenburg syndrome and related disorders of melanocyte development. Semin Cutan Med Surg 1997; 16(1):15-23.

10. NJOO MD, NIEUWEBOER-KROBOTOVA K, WESTERHOF W. Repigmentation of leucodermic defects in piebaldism by demabrasion and thin split-thickness skin grafting in combination with ninigrafting . Br J Dermatol 1998;139(5):829-33.

11. FALABELLA R, BARONA M, ESCOBAR C. Surgical combination therapy for vitiligo and piebaldism. Dermatol Surg 1995;21(10):852-7.

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