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Información de la revista
Vol. 100. Núm. 8.
Páginas 732-734 (octubre 2009)
Vol. 100. Núm. 8.
Páginas 732-734 (octubre 2009)
Clinical Science Letters
Acceso a texto completo
Patient With Malformations of the Face, Mouth, and Fingers: Type I Orofaciodigital or Papillon-Léage Psaume Syndrome
Visitas
5468
C. Ciudad
, F. Alfageme, P. Zamberk, R. Suárez
Autor para correspondencia
critxi@yahoo.es
Correspondence: Servicio de Dermatología, Hospital General Universitario Gregorio Marañón, C/ Doctor Esquerdo, 46, 28007 Madrid, Spain.
Correspondence: Servicio de Dermatología, Hospital General Universitario Gregorio Marañón, C/ Doctor Esquerdo, 46, 28007 Madrid, Spain.
Servicio de Dermatología, Hospital General Universitario Gregorio Marañón, Madrid, Spain
Este artículo ha recibido
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El Texto completo está disponible en PDF
References
[1.]
A. Patrizi, C. Orlandi, I. Neri, F. Bardazzi, G. Cocchi.
What syndrome is this? Oro-facio-digital type 1 syndrome of Papillon-Léage and Psaume.
Pediatr Dermatol, 16 (1999), pp. 329-331
[2.]
L. Pérez-Oller, R. Torra, E. Coll, F. Cofán, C. Nicolau, A. Darnell.
Síndrome orofaciodigital tipo I coexistente con enfermedad renal quística presentado en forma de insuficiencia renal crónica.
Nefrología, 19 (1999), pp. 467-471
[3.]
E. Papillon-Léage, J. Psaume.
Une malformation héréditaire de la maqueuse buccale: brides et freins anormaux.
Rev Stomatol, 55 (1954), pp. 209-227
[4.]
A.L. Ruess, S. Pruzansky, E.F. Lis, K. Patau.
The oral-facial-digital syndrome: a multiple congenital condition of females, with associated chromosomal abnormalities.
Pediatrics, 29 (1962), pp. 985-995
[5.]
F. Gurrieri, B. Franco, H. Toriello, G. Neri.
Oral-facial-digital syndromes: review and diagnostic guidelines.
Am J Med Genet, 143 (2007), pp. 3314-3323
[6.]
D.L. Rimoin, M.T. Edgerton.
Genetic and clinical heterogeneity in the oral-facial-digital syndrome.
J Pediatr, 71 (1967), pp. 94-102
[7.]
G. Anneren, B. Arvidson, K.H. Gustavson, H. Jorulf, G. Carlsson.
Oral-facial-digital syndrome I and II: radiological methods for diagnosis and the clinical variations.
Clin Genet, 26 (1984), pp. 178-186
[8.]
A. Sabato, A. Fabris, L. Oldrizzi, S. Montemezzi, G. Maschio.
Evaluation of a patient with hypertension and mild renal failure in whom facial and digital abnormalities are noted.
Nephrol Dial Transplant, 13 (1998), pp. 763-766
[9.]
D.R. Berk, S.J. Bayliss.
Milia: a review and classification.
J Am Acad Dermatol, 59 (2008), pp. 1050-1063
Copyright © 2009. Academia Española de Dermatología y Venereología and Elsevier España, S.L.