Zobrazeno 1 - 10
of 24
pro vyhledávání: '"M, Larralde de Luna"'
Autor:
M C, Boente, N, Pizzi de Parra, M, Larralde de Luna, H B, Bonet, A, Santos Muñoz, V, Parra, P, Gramajo, S, Moreno, R A, Asial
Publikováno v:
European journal of dermatology : EJD. 10(3)
The name epidermal nevus syndrome could be applied to a group of clinically and histopathologically different entities as has been pointed out by Happle. Phacomatosis pigmentokeratotica is a further type of epidermal nevus syndrome distinguished by t
Publikováno v:
Pediatric dermatology. 12(2)
We report a 1-year-old boy with an extensive cutaneous vascular malformation, oculocutaneous pigmentation, and severe neurologic abnormalities from birth, as well as a selective lgA deficiency. Ultrastructural study demonstrated prominent endothelial
Publikováno v:
Pediatric dermatology. 9(1)
A female infant was classified as having oral-facial-digital syndrome (OFDS) type 1, with oral (cleft palate, bifid uvula, lingual cleft, numerous hypertrophic frenula), facial (numerous milia on face, scalp, and ears; frontal bossing; hypertelorism;
Publikováno v:
Medicina cutanea ibero-latino-americana. 18(1)
Four cases of newborn children who presented pedal papules since birth, are reported. They showed the following features, different from the ones seen in adults: a solitary lesion, bigger size, localization on medial plantar region aspect of the heel
Publikováno v:
Pediatric Dermatology. 2:324-327
Pili trianguli canaliculi, a recently described dysmorphic disorder of the hair, occurred with variable sevenity in three related members of a family. The diagnosis was suspected from the complaint of “uncombable hair” and was confirmed by identi
Autor:
Margarita M. Larralde de Luna, Sergio Stringa, José Casas, Roberto Schroh, Irene Glikin, Julio Golberg
Publikováno v:
Pediatric dermatology. 6(3)
We cared for four patients with benign cephalic histiocytosis, a self-healing non-X, nonlipid cutaneous histiocytosis of children. The age of onset of the disease was 5 to 9 months, with papules and erythematous macules involving the head (mainly the
Publikováno v:
Revista. Circulo Argentino de Odontologia. 45(161)
Autor:
M, Larralde de Luna, R, García Díaz, G, Sánchez, R, Ilari, A M, Pierini, C, Campoy, N H, Chamoles
Publikováno v:
Medicina cutanea ibero-latino-americana. 13(2)
Fabry's disease (angiokeratoma corporis diffusum) is an X-linked recessive inherited metabolic defect due to the lack of the enzyme alpha-galactosidase A. We reviewed the Argentine literature on the subject, the main features of the disease and its d
Publikováno v:
Medicina cutanea ibero-latino-americana. 15(2)
Eleven patients with infantile acropustulosis, 10 from Mendoza and one from Buenos Aires, are presented. Remarkably was a blood eosinophilia in 4 cases and the prompt improvement with dapsone in 2 cases. The differential diagnosis with other dermatos
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