A third case of HOPP syndrome - Confirmation of the phenotype [3]

British Journal of Dermatology

Volumn 150, Issue 5, 2004, Pages 1032-1033

  Brun, A M ^a   Van Steensel, M A M ^b  

^a Hosp Univ Ruiz y Páez   (Venezuela)

^b MAASTRICHT UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

ACROOSTEOLYSIS; ADULT; CASE REPORT; CLINICAL FEATURE; DISEASE COURSE; FAMILY HISTORY; HUMAN; HYPOTRICHOSIS; KERATOSIS PALMOPLANTARIS; LABORATORY TEST; LETTER; MALE; PERIODONTITIS; PHENOTYPE; PRIORITY JOURNAL; NAIL DISEASE; SYNDROME;

ADULT; HUMANS; HYPOTRICHOSIS; KERATODERMA, PALMOPLANTAR; MALE; NAILS, MALFORMED; PHENOTYPE; SYNDROME;

EID: 3042820961     PISSN: 00070963     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1365-2133.2004.05939.x     Document Type: Letter

References (4)

1. Van Steensel MA, Van Geel M, Steijlen PM. New syndrome of hypotrichosis, striate palmoplantar keratoderma, acro-osteolysis and periodontitis not due to mutations in cathepsin C. Br J Dermatol 2002; 147: 575-81.
2. Kopysc Z, Barczyk K, Krol E. A new syndrome in the group of euhidrotic ectodermal dysplasia. Pilodental dysplasia with refractive errors. Hum Genet 1985; 70: 376-8.
3. Xing QH, Wang MT, Chen XD et al. A gene locus responsible for dyschromatosis symmetrica hereditaria (DSH) maps to chromosome 6q24.2-q25.2. Am J Hum Genet 2003; 73: 377-82.
4. Zhang XJ, Gao M, Li M et al. Identification of a locus for dyschromatosis symmetrica hereditaria at chromosome 1q11-1q21. J Invest Dermatol 2003; 120: 776-80.