Journal Information
Vol. 56. Issue 5.
Pages 473-474 (1 May 2002)
Vol. 56. Issue 5.
Pages 473-474 (1 May 2002)
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Síndrome de schwartz-jampel tipo 2 frente a síndrome de stüve-wiedemann
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F.E. Navarrete Faubela,
Corresponding author
enavarretef@yahoo.es

Correspondencia: Joaquín Ballester, 8, pta. 5. 46009 Valencia
, A. Pérez Aytésb, J. Pastor Rosadoc, A. Mascarell Gregoria
a Servicios de Ortopedia y Traumatología
b Servicios de Neonatología. Hospital Universitario La Fe. Valencia.
c Servicio de Pediatría. Hospital Vega Baja. Orihuela.
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Bibliografía
[1.]
L. Al-Gazali, M. Varghese, E. Varady, J. Al Talabani, J. Scorer, D. Bakalinova.
Neonatal Schwartz-Jampel syndrome: A common autosomal recessive syndrome in the United Arab Emirates.
J Med Genet, 33 (1996), pp. 203-211
[2.]
V. Cormier-Daire, A. Munnich, S. Lyonnet, et al.
Presentation of six cases of Stüve-Wiedemann syndrome.
Pediatr Radiol, 28 (1998), pp. 776-780
[3.]
V. Cormier-Daire, A. Superti-Fuga, A. Munnich, et al.
Clinical homogeneity of the Stüve-Wiedemann syndrome and overlap with the Schwartz-Jampel syndrome type 2.
Am J Med Genet, 78 (1998), pp. 146-149
[4.]
S. Sigaudy, A. Moncla, C. Fredouille, B. Bourlière, J.C. Lambert, N. Philip.
Congenital Bowing of the long bones in two fetuses presenting features of Stüve-Wiedemann syndrome and Schwartz-Jampel syndrome type 2.
Clinical Dysmorphology, 7 (1998), pp. 257-262
[5.]
A. Superti-Fuga, R. Tenconi, M. Clementi, et al.
Schwartz-Jampel syndrome type 2 and Stüve-Wiedemann syndrome: A case for “lumping”.
Am J Med Genet, 30 (1998), pp. 150-154
Copyright © 2002. Asociación Española de Pediatría
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