The expanding spectrum of Galli-Galli disease

Journal of the American Academy of Dermatology

Volumn 56, Issue 5 SUPPL., 2007, Pages

  El Shabrawi Caelen, Laila ^a   Rütten, Arno ^b   Kerl, Helmut ^a  

^a UNIVERSITY OF GRAZ   (Austria)

^b Histologisches Gemeinschaftslabor   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

RETINOID; STEROID;

AGED; ANAMNESIS; ARTICLE; CASE REPORT; CLINICAL FEATURE; FAMILY HISTORY; FEMALE; GALLI GALLI DISEASE; GENODERMATOSIS; HUMAN; HUMAN TISSUE; PHOTOTHERAPY; PRIORITY JOURNAL; SKIN BIOPSY;

ACANTHOLYSIS; AGED; CHROMOSOMES, HUMAN, PAIR 12; DIAGNOSIS, DIFFERENTIAL; FEMALE; GENES, DOMINANT; HUMANS; KERATIN-5; MUTATION; PIGMENTATION DISORDERS; SKIN;

EID: 34047260575     PISSN: 01909622     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jaad.2006.10.987     Document Type: Article

References (16)

1. Dowling G., and Freudenthal W. Acanthosis nigricans. Br J Dermatol 50 (1938) 467-471
2. Degos R., and Ossipowski B. Reticulated pigmentary dermatosis of the folds: relation to acanthosis nigricans (in French). Ann Dermatol Syphiligr (Paris) 81 (1954) 147-151
3. Wilson Jones E., and Grice K. Reticulated pigmented anomaly of the flexures. Arch Dermatol 114 (1978) 1150-1157
4. Betz R.C., Planko L., Eigelshoven S., Hanneken S., Pasternack S.M., Bussow H., et al. Loss-of-function mutations in the keratin 5 gene lead to Dowling-degos disease. Am J Hum Genet 78 (2006) 510-519
5. Gebhart W., Bardach H., and Niebauer G. A peculiar genodermatosis in two brothers: Dowling-Degos, Grover, Darier, Hailey-Hailey disease or "Morbus Galli-Galli"? (abstract) (1981), Society for Cutaneous Ultrastructure Research, London p. XV
6. Bardach H., Gebhart W., and Luger T. Genodermatosis in a pair of brothers: Dowling-Degos, Grover, Darier, Hailey-Hailey or Galli-Galli disease?. [in German]. Hautarzt 33 (1982) 378-383
7. Kitamura K., and Akamatsu S. Eine besondere Form der Akropigmentation: acropigmentatio reticularis. Rinsho No Hifu Hitsunyo. 1943:201. Quoted by Griffiths WAD. Reticulate Acropigmentation of Kitamura. Br J Dermatol 95 (1976) 437-443
8. Sanderson K.V., and Wilson H. Haber's syndrome: familial rosacea-like eruption with intraepidermal epithelioma. Br J Dermatol 77 (1965) 1-8
9. Mittag H., Rupec M., and Klingmüller G. Der Morbus Galli-Galli - eine Entität?. Akt Dermatol 12 (1986) 41-46
10. Rütten A., and Strauß T. Morbus Galli-Galli: a further case report. Akt Dermatol 21 (1995) 255-257
11. De Deene A., and Schulze H. Morbus Galli-Galli: eine Variante des Morbus Darier?. H + G Zeitschrift für Hautkrankheiten 71 (1996) 860-862
12. Braun-Falco M., Volgger W., Borelli S., Ring J., and Disch R. Galli-Galli disease: an unrecognized entity or an acantholytic variant of Dowling-Degos disease?. J Am Acad Dermatol 45 (2001) 760-763
13. Cramer H. Verrucosis seborrhoica. Hautarzt 20 (1969) 31-34
14. Kaminsky C., De Kaminsky A., Sanguinetti O., and Shaw M. Acquired pigmentation of skin folds with the histologic picture of seborrheic wart. Br J Dermatol 93 (1975) 713-716
15. Cooper S.M., Dhittavat J., Millard P., and Burge S. Extensive Grover's-like eruption with lentiginous 'freckling': report of two cases. Br J Dermatol 150 (2004) 350-352
16. Girard C., Durand L., Guillot B., Gildhou J.J., and Bessis D. Persistent acantholytic dermatosis and extensive lentiginous 'freckling': a new entity?. Br J Dermatol 153 (2005) 217-218