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First International Symposium of Myelodysplastic Syndromes Innsbruck, June 20–23, 1988

First International Symposium of Myelodysplastic Syndromes Innsbruck, June 20–23, 1988 Blut (1988) 56:C1-C23 Blur © Springer-Verlag 1988 First International Symposium on Myelodysplastic Syndromes Innsbruck, June 20-23, 1988 Abstracts Abstracts of papers selected for poster presentation Abstracts of papers selected for oral presentation C3-C18 C19-C23 Springer International PI REPORT AR)UT A CASE OF "FAMILIAL" MYELODYSPI~k~IC S P ~ D R ~ ( ~DS ) S. Nardelli, F. Ciccone, A. M~desti, E. Cupellaro & L. Deriu In November 1986 we identified a fanily in which 3 sisters ( 25, 23, 19 yrs. old respectively ) were affected by l~)S, strangely associated with severe iron deficiency~ lack in vit B]2 and folate, gastric mnlabsorption, whereas blood picture in their parents was substantially normal. Since clinical features and haematologic parameters at presentation were strictly similar, we s~mmrize the more characteristic data jointly : - Severe hypochromic microcytic anaemia, with Hb*=6 g/dl in 2/3 - Reticulocytes, Neutrophils and Platelets count under average, very low in the eldest sister - Research for thalassaemia, other hereditary haemolytic disorders, Ham - Dacie test : all negative - Auto-ianunity tests : all negative, except for AWA, detectable in 2/3 - Bone-n~rrow smears and biopsies : hypercellularity, morphologic abnormalities in each cell line and presence of blasts variable http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Annals of Hematology Springer Journals

First International Symposium of Myelodysplastic Syndromes Innsbruck, June 20–23, 1988

Annals of Hematology , Volume 56 (6) – Jun 1, 1988

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Publisher
Springer Journals
Copyright
Copyright © 1988 by Springer-Verlag
Subject
Medicine & Public Health; Hematology; Oncology
ISSN
0939-5555
eISSN
1432-0584
DOI
10.1007/BF00320292
Publisher site
See Article on Publisher Site

Abstract

Blut (1988) 56:C1-C23 Blur © Springer-Verlag 1988 First International Symposium on Myelodysplastic Syndromes Innsbruck, June 20-23, 1988 Abstracts Abstracts of papers selected for poster presentation Abstracts of papers selected for oral presentation C3-C18 C19-C23 Springer International PI REPORT AR)UT A CASE OF "FAMILIAL" MYELODYSPI~k~IC S P ~ D R ~ ( ~DS ) S. Nardelli, F. Ciccone, A. M~desti, E. Cupellaro & L. Deriu In November 1986 we identified a fanily in which 3 sisters ( 25, 23, 19 yrs. old respectively ) were affected by l~)S, strangely associated with severe iron deficiency~ lack in vit B]2 and folate, gastric mnlabsorption, whereas blood picture in their parents was substantially normal. Since clinical features and haematologic parameters at presentation were strictly similar, we s~mmrize the more characteristic data jointly : - Severe hypochromic microcytic anaemia, with Hb*=6 g/dl in 2/3 - Reticulocytes, Neutrophils and Platelets count under average, very low in the eldest sister - Research for thalassaemia, other hereditary haemolytic disorders, Ham - Dacie test : all negative - Auto-ianunity tests : all negative, except for AWA, detectable in 2/3 - Bone-n~rrow smears and biopsies : hypercellularity, morphologic abnormalities in each cell line and presence of blasts variable

Journal

Annals of HematologySpringer Journals

Published: Jun 1, 1988

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