Darier´s disease. Presentation of a family

Authors

  • Irene Ayala Rosales HOPITAL PROVINCIAL UNIVERSITARIO “CARLOS MANUEL DE CÉSPEDES” BAYMO
  • Alicia La O Cabrera HOPITAL PROVINCIAL UNIVERSITARIO “CARLOS MANUEL DE CÉSPEDES” BAYMO
  • Electra Guerra Domínguez HOPITAL PROVINCIAL UNIVERSITARIO “CARLOS MANUEL DE CÉSPEDES” BAYMO
  • Yadira La O Ayala HOPITAL PROVINCIAL UNIVERSITARIO “CARLOS MANUEL DE CÉSPEDES” BAYMO
  • Maria Esther Martínez Guerra HOPITAL PROVINCIAL UNIVERSITARIO “CARLOS MANUEL DE CÉSPEDES” BAYMO

Keywords:

KERATOSIS FOLLICULARIS /genetics, KERATOSIS FOLLICULARIS /diagnosis, BIOPSY, SKIN / pathology, SKIN DISEASES /pathology

Abstract

Darier´s disease is a dominant autosomal disorder, by altered keratinization of the epidermis, nails and mucosa; it is clinically characterized by the presence of papulokeratotic lesions, mainly folliculars, that predominate in seborrhoeic zones. It was presented a family that have followed this heritage model with refered cases and two confirmed by the clinic and the histology with very similar expressions in the clinical characteristics and torpid evolution with symptoms of frequent aggravated symptoms. Case 1 ROB (lll-11) of 45 years old and the Case 2 DOR (lV-8) of 14 years old, both father and daughter, it was made a bibliographic revision of the entity.

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References

1. Darier J. La psorospermose folliculaire vegetante. Ann Dermatol Syphiligr 1889; 10: 597-612.

2. Jorda E, Revert A, Montesinos E, Zayas A. Unilateral Darier´s disease. Int Dermatol 1996;

35: 288-289.

3. Fernández Hernández Vaquero G. Enfermedad de Darier. En; Dermatología. La Habana: Ed.

Científico Técnica;1986, p.135-139.

4. Nakagawa T, Masada M, Moriue T, Takaiwa T. Comedo-like acantholytic dyskeratosis of the

face and scalp: a new entity? Br J Dermatol 2000; 142: 1047-1048.

5. Katta R, Reed J. Wolf JE. Cornifying Darier´s disease. Int Dermatol 2000; 39: 844-845.

6. Peterson CM, Lesher JL Jr, Sangueza OP. A unique variant of Darier´s disease. Int J

Dermatol 2001; 40: 278-280.

7. Telfer NR, Burge SM, Ryan TJ. Vesiculo-bullous Darier's disease. Br J Dermatol 1990; 122:

831-834.

8. Hellwig B, Hesslinger B, Walden J. Darier's disease and psychosis. Psychiatry Res 1996; 64:

205-207.

9. Aleyda Urquiza, Leopoldina, Braulio Zayas y Eraida Hernández. Acroqueratosis Verrusiforme

diagnosticada en un adulto. Presentación de un caso. Rev Cuban Med Milit. 2002; 31(4).

10. Silvestre Martínez, Angel Vera. Carmen Eloy-García, Andrés Sanz, Vicente Crespo.

Enfermedad de DarierLinial. Actas Dermosifiliogr. 2006; 97:139-41.

11. R Ruiz-Villaverde, J Blasco Melguizo, AC Menéndez García Estrada, MC Jiménez Cortés. F

Díez García. Enfermedad de Darier unilateral y segmentaria tipo I.An Pediatr (Barc). 2004;

60:92-4.

12.Vínculos a catálogo McKusick: 124200 Código CIE-9-MC: 757.39

13. http://www.fundacion1000.es/ consultado nov./ 2007.

14. info@enfermedades-raras.org

http://www.enfermedades-raras.org/es/default.htm

15. Correo-e : eurordis@eurordis.org http://www.eurordis.org

16. Manssur I, Díaz Almeida. Genodermatosis. En: Díaz Almeida J. Dermatología. La Habana:

Editorial Ciencias Médicas;2002, 48:50.

17. Eva Cavaría, José M Hernández. Placas erosivas y verrugosas en pliegues inguinales.

Actas Dermosifiliogr. 2005;96:703-5.

Published

2008-07-13

How to Cite

1.
Ayala Rosales I, La O Cabrera A, Guerra Domínguez E, La O Ayala Y, Martínez Guerra ME. Darier´s disease. Presentation of a family. RM [Internet]. 2008 Jul. 13 [cited 2025 Jun. 3];12(3). Available from: https://revmultimed.sld.cu/index.php/mtm/article/view/1837

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Section

CASOS CLÍNICOS