A sporadic case of Mal de Meleda caused by gene mutation in SLURP-1 in Korea

Annals of Dermatology

Volumn 23, Issue 3, 2011, Pages 396-399

  Oh, Young Jae ^a   Lee, Ha Eun ^a   Ko, Joo Yeon ^a   Ro, Young Suck ^a   Yu, Hee Joon ^a  

^a Hanyang University   (South Korea)

Author keywords

Mal de Meleda; Palmoplantar keratoderma; SLURP 1; Transgrediens

Indexed keywords

EID: 80052094263     PISSN: 10139087     EISSN: None     Source Type: Journal    
DOI: 10.5021/ad.2011.23.3.396     Document Type: Article

References (9)

1. Wajid M, Kurban M, Shimomura Y, Christiano AM. Mutations in the SLURP-1 gene underlie Mai de Meleda in three Pakistani families. J Dermatol Sci 2009;56:27-32.
2. Chao SC, Lai FJ, Yang MH, Lee JY. Mai de Meleda in a taiwanese. J Formos Med Assoc 2005;104:276-278.
3. Ergin S, Erdogan BS, Aktan S. Mai de Meleda: a new geographical localization in Anatolia. Dermatology 2003;206:124-130. (Pubitemid 36205279)
4. Kelsell DP, Stevens HP. The palmoplantar keratodermas: much more than palms and soles. Mol Med Today 1999;5:107-113. (Pubitemid 29282264)
5. Saftić V, Rudan D, Zgaga L. Mendelian diseases and conditions in Croatian island populations: historic records and new insights. Croat Med J 2006;47:543-552. (Pubitemid 44285481)
6. Fischer J, Bouadjar B, Heilig R, Huber M, Lefèvre C, Jobard F, et al. Mutations in the gene encoding SLURP-1 in Mai de Meleda. Hum Mol Genet 2001;10:875-880. (Pubitemid 32331598)
7. Chimienti F, Hogg RC, Plantard L, Lehmann C, Brakch N, Fischer J, et al. Identification of SLURP-1 as an epidermal neuromodulator explains the clinical phenotype of Mai de Meleda. Hum Mol Genet 2003;12:3017-3024. (Pubitemid 37442029)
8. Katugampola RP, Finlay AY. Oral retinoid therapy for disorders of keratinization: single-centre retrospective 25 years' experience on 23 patients. Br J Dermatol 2006;154:267-276. (Pubitemid 43382697)
9. Braun-Falco M. Hereditary palmoplantar keratodermas. J Dtsch Dermatol Ges 2009;7:971-984.