A severe transfusion-dependent congenital dyserythropoietic anemia presenting as hydrops fetalis

British Journal of Haematology

Volumn 96, Issue 3, 1997, Pages 530-533

  Cantu Rajnoldi A ^a,d   Zanella, A ^b   Conter, U ^c   Faccini, P ^c   Soligo, D ^b   Gornati, G ^a   Vegni, C ^c   Nicolini, U ^c  

^a Istituti Clinici di Perfezionamento   (Italy)

^b FONDAZIONE IRCCS CA GRANDA OSPEDALE MAGGIORE POLICLINICO   (Italy)

^c UNIVERSITY OF MILAN   (Italy)

^d IPC   (Italy)

Author keywords

Congenital dyserythropoietic anaemia; Fetal hydrops

Indexed keywords

ANEMIA; ARTICLE; BLOOD TRANSFUSION; CASE REPORT; DYSERYTHROPOIESIS; ELECTRON MICROSCOPY; FETUS; FETUS HYDROPS; HUMAN; PRIORITY JOURNAL;

ADULT; ANEMIA, DYSERYTHROPOIETIC, CONGENITAL; BLOOD TRANSFUSION; ERYTHROBLASTOSIS, FETAL; FEMALE; HUMANS; HYDROPS FETALIS; INFANT, NEWBORN; MICROSCOPY, ELECTRON; PREGNANCY;

EID: 0031030351     PISSN: 00071048     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-2141.1997.d01-2062.x     Document Type: Article

References (10)

1. Boogaerts, M.A. & Verwilghen, R.L. (1982) Variant of congenital dyserythropoietic anaemia: an update. Haematologia, 15, 211-219.
2. Carter, C., Darbyshire, P.J. & Wickramasinghe, S.N. (1989) A congenital dyserythropoietic anaemia variant presenting as hydrops foetalis. British Journal of Haematology, 72, 289-290.
3. Fairbanks, G., Speck, T.L. & Wallach, D.F.G. (1971) Electrophoretic analysis of the major polypeptides of the human erythrocyte membrane. Biochemistry, 10, 2606-2617.
4. Fukuda, M.N. (1993) Congenital dyserythropoietic anaemia type II (HEMPAS) and its molecular basis. Baillieres Clinical Haematology, 6, 493-511.
5. Heimpel, H. & Wendt, F. (1968) Congenital dyserythropoietic anaemia with karyorexis and multinuclearity of erythroblasts. Helvetica Medica Acta, 34, 103-115.
6. Laemli, U.K. (1970) Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature, 227, 680-685.
7. Roberts, D.J., Nadel, A., Lage J. & Rutherford, C.J. (1993) An unusual variant of congenital dyserythropoietic anaemia with mild maternal and lethal foetal diseases. British Journal of Haematology, 84, 549-551.
8. Sansone, G., Masera, G., Cantù-Rajnoldi, A. & Terzoli, S. (1992) An unclassified case of congenital dyserythropoietic anaemia with a severe neonatal onset. Acta Haematologica, 88, 41-5.
9. Scartezzini, P., Forni, G.L., Baldi, M., Izzo, C. & Sansone. G. (1982) Decreased glycosylation of band 3 and band 4.5 glycoproteins of erythrocyte membrane in congenital dyserythropoietic anaemia type II. British Journal of Haematology, 51, 569-576.
10. Williams, G., Lorimer, S., Merry, C.C., Greenberg, C.R. & Bishop, A.J. (1990) A variant congenital dyserythropoietic anaemia presenting as a fatal hydrops foetalis. (Letter). British Journal of Haematology, 76, 438-439.