medigraphic.com
SPANISH

Revista del Centro Dermatológico Pascua

ISSN 1405-1710 (Print)
  • Contents
  • View Archive
  • Information
    • General Information        
    • Directory
  • Publish
    • Instructions for authors        
  • medigraphic.com
    • Home
    • Journals index            
    • Register / Login
  • Mi perfil

2010, Number 3

<< Back Next >>

Rev Cent Dermatol Pascua 2010; 19 (3)

Reticulate acropigmentation of Dohi in two brothers

Jiménez HF, Martínez ZM, Ramos A, Santa CFJ
Full text How to cite this article

Language: Spanish
References: 13
Page: 123-126
PDF size: 353.68 Kb.


Key words:

Reticulate acropigmentation of Dohi, reticulate acropigmentation, dyschromatosis symmetric.

ABSTRACT

Reticulate acropigmentation of Dohi is a rare disorder in Latin America; this condition is characterized by hypopigmented macules in dorsum of hand and feet. It presents a dominant autosomic herence. There are mutations in the melanin production gen. The differential diagnostic is reticulate acropigmentation of Kitamura. There is no specific treatment. The present article presents a brother and sister with acropigmented reticulate Dohi without familiar antecedents.


REFERENCES

  1. López ZI, Navarrete FG, Jurado SCF. Acropigmentación reticulada de Dohi. Dermatol Rev Mex 2008; 52: 231-234.

  2. Ortone J, Bahadoran P, Fitzpatrick T et al. Hipomelanosis e hipermelanosis. En: Freedberg, Eisen, Wolff, et al, Fitzpatrick Dermatología en Medicina General. Argentina, 2005; 2: 977.

  3. Kono M, Miyamura Y, Matsunaga J, Tomita Y. Exclusion of linkage between dyschromatosis symmetric hereditary and chromosome 9. J Dermatol Sci 2000; 22: 88-95.

  4. Mari J, Escutia B, Febrer S. Reticulate acropigmentation of Dohi. Actas Dermo-Sifiliográficas 2001; 92: 288-290.

  5. Álvarez P, Ramos C, Salomón M. et al. Acropigmentación reticulada de Dohi. Folia Dermatol 2007; 18: 42-44.

  6. Trout C, Levine N, Wu Chang M. Trastornos de hiperpigmentación. En: Bolognia L, Jorizzo J, Rapini R. Dermatología. Madrid, España; Elsevier, 2004; 1: 1001-1002.

  7. Consigli J, Gómez M, Ragazzini L et al. Dyschromatosis symmetric hereditary: report of a sporadic case. Int J Dermatol 2010; 10: 918-920.

  8. Santos R, Beltrán G, Meza B et al. Presentación inusual de un caso de acropigmentación reticulada de Kitamura. Dermatol Perú 2003; 13: 231-233.

  9. Eichenfield L. Dermatologic Neonatal. España; Elsevier, 2009: 550.

  10. Miyamura Y, Suzuki, Kono M. Mutations of the RNA-specific adenosine deaminase gene (DSRAD) are involved in dyschromatosis symmetric hereditary. Am J Hum Genet 2003; 73: 693-699.

  11. Danese P, Zanca A, Bertazzoni MG. Familial reticulate acropigmentation of Dohi. J Am Acad Dermatol 1997; 37: 884-886.

  12. Schnur RE, Heymann WR. Reticulate hyperpigmentation. Semin Cutan Med Surg 1997; 16: 72-80.

  13. Cammarata-Scalisi F, Caraballo Y, Reyes O et al. Enfermedad de Dowling-Degos asociada con carcinoma basocelular: Reporte de un caso con hallazgos clínicos inusuales. Dermatol Perú 2004; 14: 208-210.




2020     |     www.medigraphic.com

Mi perfil

C?MO CITAR (Vancouver)

Rev Cent Dermatol Pascua. 2010;19