Concordance of striate palmoplantar keratoderma and brachyphalangia in monozygous twins [11]

Journal of the European Academy of Dermatology and Venereology

Volumn 20, Issue 10, 2006, Pages 1343-1345

  Tursen, U ^a   Ustunsoy, D ^a   Api, H ^a   Polat, A ^a   Ikizoglu, G ^a  

^a MERSIN UNIVERSITY   (Turkey)

Author keywords

[No Author keywords available]

Indexed keywords

SALICYLIC ACID; UREA;

BONE DISEASE; BONE RADIOGRAPHY; BRACHYPHALANGY; CASE REPORT; CLINICAL PROTOCOL; CONGENITAL MALFORMATION; DIAGNOSTIC PROCEDURE; FEMALE; HOSPITAL ADMISSION; HUMAN; HUMAN TISSUE; KERATOSIS PALMOPLANTARIS; LETTER; METATARSAL BONE; MONOZYGOTIC TWINS; PRESCRIPTION; PRIORITY JOURNAL; SCHOOL CHILD; SKIN BIOPSY; SKIN EXAMINATION;

CHILD; DISEASES IN TWINS; FEMALE; FOOT DEFORMITIES, CONGENITAL; HUMANS; KERATODERMA, PALMOPLANTAR; METATARSAL BONES; TWINS, MONOZYGOTIC;

EID: 33750340978     PISSN: 09269959     EISSN: 14683083     Source Type: Journal    
DOI: 10.1111/j.1468-3083.2006.01690.x     Document Type: Letter

References (9)

1. Rickman L, Simrak D, Stevens HP et al. N-terminal deletion in a desmosomal cadherin causes the autosomal dominant skin disease striate palmoplantar keratoderma. Hum Mol Genet 1999; 8: 971-976.
2. Armstrong D, McKenna KE, Purkis PE et al. Haploinsufficiency of desmoplakin causes a striate subtype of palmoplantar keratoderma. Hum Mol Genet 1999; 8: 143-148.
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