[PDF] from medicaljournals.seM Glatz, MAM van Steensel, M van Geel… - 2011 - medicaljournals.se Erythrokeratodermia variabilis (EKV, MIM ID #133200) is a rare congenital disorder, usually inherited as an auto- somal dominant trait (1). EKV is clinically characterized by two morphological features; namely, more-or-less fixed hyperkeratoses and variable and transient red pat- ... Related articles - View as HTML
Z Wang - Journal of the European Academy of Dermatology …, 2011 - Wiley Online Library ... A novel GJB3 (Cx31) missense mutation in a Chinese patient with erythrokeratodermia variabilis. ZX Wang 1,2,3,† ,; WS Lu 1,2,† ,; H Li 1,3 ,; D Lin 1,3 ,; FS Zhou 1,2 ,; LD Sun 1,2,3 ,; S Yang 1,2,3 ,; XJ Zhang 1,2,3,*. Article first published online: 28 JUN 2010. ... All 2 versions
HM Nam, UK Kim, K Park… - Korean Journal of Dermatology, 2011 - komci.org Erythrokeratodermia variabilis is a rare genodermatosis characterized by the coexistence of randomly occurring, transient, erythematous patches and hyperkeratosis of the skin. A 25-year-old Uzbekistanian female with congenital deaf-mutism presented with well ... Cached - All 2 versions
P Kumar… - Indian pediatrics, 2011 - ncbi.nlm.nih.gov 1. Indian Pediatr. 2011 Apr 7;48(4):337-8. Progressive symmetric Erythrokeratodermia. Kumar P, Mondal A. Department of Dermatology and STD Medical College and Hospital Kolkata 700 073, West Bengal, India. PMID: 21532109 [PubMed - in process].
P symmetric Erythrokeratodermia - Indian Pediatr, 2011 - indianpediatrics.net A 3-years-old female child presented with asymptomatic multiple well-defined erythematous scaly plaques since infancy. She was born of a non-consanguineous marriage and had uneventful prenatal and natal period. The lesions started appearing in first few months of life first on ... Cached