Search Results - "Larralde de Luna, M"

Oral-facial-digital type 1 syndrome of Papillon-Léage and Psaume by Larralde de Luna, M, Raspa, M L, Ibargoyen, J

“…A female infant was classified as having oral-facial-digital syndrome (OFDS) type 1, with oral (cleft palate, bifid uvula, lingual cleft, numerous hypertrophic…”
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Pedal papules in newborn infants by Larralde de Luna, M, Ruiz León, J, Cabrera, H N

“…Four cases of newborn children who presented pedal papules since birth, are reported. They showed the following features, different from the ones seen in…”
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Infantile acropustulosis. Considerations on 11 cases by Pizzi de Parra, N, Larralde de Luna, M, Cicioni, V, Parra, C A

“…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…”
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Phacomatosis pigmentokeratotica : another epidermal nevus syndrome and a distinctive type of twin spotting by DEL C. BOENTE, M, PIZZI DE PARRA, N, LARRALDE DE LUNA, M, BIBAS BONET, H, SANTOS MUNOZ, A, PARRA, V, GRAMAJO, P, MORENO, S, ASIAL, R. A

“…The name epidermal nevus syndrome could be applied to a group of clinically and histopathologically different entities as has been pointed out by Happle…”
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Angiokeratoma corporis diffusum (Fabry's disease). Update. Apropos of 2 cases by Larralde de Luna, M, García Díaz, R, Sánchez, G, Ilari, R, Pierini, A M, Campoy, C, Chamoles, N H

“…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…”
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Phacomatosis pigmentovascularis with a selective IgA deficiency by de Luna, M L, Barquin, M A, Casas, J G, Sidelsky, S

“…We report a 1-year-old boy with an extensive cutaneous vascular malformation, oculocutaneous pigmentation, and severe neurologic abnormalities from birth, as…”
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Pili trianguli canaliculi: uncombable hair syndrome in a family with apparent autosomal dominant inheritance by de Luna, M M, Rubinson, R, de Kohan, Z B

“…Pili trianguli canaliculi, a recently described dysmorphic disorder of the hair, occurred with variable severity in three related members of a family. The…”
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Benign cephalic histiocytosis: report of four cases by de Luna, M L, Glikin, I, Golberg, J, Stringa, S, Schroh, R, Casas, J

“…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…”
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Ectodermal dysplasia and its orodental rehabilitation by Martin de Kramer, N E, Larralde de Luna, M, Ravaglia, C

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Umbilical polyps by Larralde de Luna, M, Cicioni, V, Herrera, A, Casas, J G, Magnin, P H

“…We report three patients, ages 5 years, 3 years, and 4 days, with umbilical polyps. In the third child the polyp was associated with an umbilical enteric…”
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