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Autor:
Patrícia A. Couto, Marcela C. Pastore, Jessica C. N. Araújo, Cecilya M. Mota, Caroline A. R. Chirano, Valeria K. A. Ferreira, Sidharta Q. Gadelha, Elaine D. Melo, Patricia C. B. de Melo, Luciana M. Santos
Publikováno v:
Revista da Sociedade Portuguesa de Dermatologia e Venereologia, Vol 77, Iss 1 (2019)
Harlequin ichthyosis is a rare autosomal recessive congenital disease in which neonates present generalized hyperkeratotic plaques and deep fissures, ectropion, eclabium, malformation of the auricular pavilion and typical facies. Although several com
Externí odkaz:
https://doaj.org/article/cb80a0a46716480395a4f4a1418e0f6c