Imerslund-Grasbeck SyndromeNihal Karatoprak, Ayla Karatürk, Serpil Yavrucu, Ahmet ÖzgünerHaydarpasa Numune Hospital Pediatric Clinic, Istanbul
Imerslund-Grasbeck syndrome is an uncommon, hereditary disease, characterized by megaloblastic anemia and proteinuria. A two-year-old boy with the characteristic findings is
described in our Clinic. Replacement therapy with parenteral vitamin B12 resulted in remarkable clinical and haematological improvement. Keywords: Megaloblastic anemia, Imerslund-Grasbeck syndrome
Imerslund-Grasbeck SendromuNihal Karatoprak, Ayla Karatürk, Serpil Yavrucu, Ahmet ÖzgünerHaydarpaşa Numune Hastanesi Çocuk Kliniği, İstanbul
Anahtar Kelimeler: Megaloblastik anemi, Imerslund-Grasbeck sendromu
Nihal Karatoprak, Ayla Karatürk, Serpil Yavrucu, Ahmet Özgüner. Imerslund-Grasbeck Syndrome. Medeniyet Med J. 2001; 16(3): 186-187
Corresponding Author: Nihal Karatoprak, Türkiye |
|