An uncommon cause of linfadenopathy in a kidney transplant patient: cat-scratch disease.

نویسندگان

  • Cláudia Bento
  • La Salete Martins
  • André Coelho
  • Manuela Almeida
  • Sofia Pedroso
  • Leonídeo Dias
  • Ramon Vizcaíno
  • António Castro-Henriques
  • António Cabrita
چکیده

Nefrologia 2014;34(4):xx 15 ed presentation of methylmalonic aciduria and hyperhomocystinuria, cblC type. Prenat Diagn 2009;29:266-70. 3. Rogé Canales M, Rodrigo Gonzalo de Liria C, Prats Viñas LJ, Vaquero Pérez M, Ribes Rubió A, Rodés Monegal M, et al. Síndrome hemolítico-urémico neonatal asociado a aciduria metilmalónica y homocistinuria. An Esp Pediatr 1996;45:97-8. 4. Menni F, Testa S, Guez S, Chiarelli G, Alberti L, Esposito S. Neonatal atypical hemolytic uremic syndrome due to methylmalonic aciduria and homocystinuria. Pediatr Nephrol 2012;27:1401-5. 5. Huemer M, Simma B, Fowler B, Suormala T, Bodamer OA, Sass JO. Prenatal and postnatal treatment in cobalamin C defect. J Pediatr 2005;147:469-72.

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عنوان ژورنال:
  • Nefrologia : publicacion oficial de la Sociedad Espanola Nefrologia

دوره 34 4  شماره 

صفحات  -

تاریخ انتشار 2014