T Narita, N Oiso, K Fukai, T Motokawa… - European journal of …, 2011 - ncbi.nlm.nih.gov 1. Eur J Dermatol. 2011 Jun 16. [Epub ahead of print] Two children with a mild or moderate piebaldism phenotype and a father without leukoderma in a family with the same recurrent missense mutation in the kinase domain of KIT. ...
V López… - Dermatology online journal, 2011 - ncbi.nlm.nih.gov 1. Dermatol Online J. 2011 Feb 15;17(2):13. Piebaldism in a 2-year-old girl. López V, Jordá E. Departments of Dermatology, Hospital Clínico Universitario de Valencia, Valencia, Spain. ebaldism is a rare autosomal dominant ...
[HTML] from cdlib.orgMD Verónica López - Dermatology Online Journal, 2011 - dermatology.cdlib.org A 2-year-old girl, with no relevant medical history, was referred to our department for evaluation of a white forelock and white patches over the trunk, upper extremities and lower extremities. Her mother informed us that the white forelock was present since birth, whereas the white ... Related articles - Cached - All 2 versions
[HTML] from nih.govN van Geel, BK Goh, E Wallaeys… - Journal of cutaneous …, 2011 - ncbi.nlm.nih.gov ... Only the clinical trials on non-cultured epidermal cellular grafting (using trypsin) for vitiligo (segmental, generalized, mixed) and in addition, other types of leucoderma (halo nevi, nevus depigmentosus, chemical leucoderma, piebaldism) were included. ... Related articles - All 6 versions
[HTML] from ijsronline.comG Singh, K Ahya, DY Shrikhande, S Patil… - … Journal of Students' …, 2011 - ijsronline.com ... Key Words: Waardenburg syndrome, white forelock, sensorineural deafness, Piebaldism. Introduction. ... With this view, a differential diagnosis of Waardenburg syndrome and Piebaldism was made on initial clinical assessment. ... Related articles - Cached - All 5 versions