Imerslund-Grasbeck Syndrome
Nihal Karatoprak, Ayla Karatürk, Serpil Yavrucu, Ahmet ÖzgünerHaydarpasa Numune Hospital Pediatric Clinic, IstanbulImerslund-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.
Imerslund-Grasbeck Sendromu
Nihal Karatoprak, Ayla Karatürk, Serpil Yavrucu, Ahmet ÖzgünerHaydarpaşa Numune Hastanesi Çocuk Kliniği, İstanbulAnahtar Kelimeler: Megaloblastik anemi, Imerslund-Grasbeck sendromu
Nihal Karatoprak, Ayla Karatürk, Serpil Yavrucu, Ahmet Özgüner. Imerslund-Grasbeck Syndrome. . 2001; 16(3): 186-187
Corresponding Author: Nihal Karatoprak, Türkiye
Corresponding Author: Nihal Karatoprak, Türkiye
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