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http://hdl.handle.net/123456789/2410
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| Title: | SFEROCITOZA EREDITARĂ LA NOU-NĂSCUT – PREZENTARE DE CAZ |
| Other Titles: | HEREDITARY SPHEROCYTOSIS IN NEWBORN – CASE REPORT |
| Authors: | Păltinişanu, Emanuela
Vodă, Daniela
Falup-Pecurariu, Oana |
| Keywords: | hereditary spherocytosis
diagnosis
newborn
haemolytic crisis |
| Issue Date: | 2015 |
| Publisher: | Editura Universității Transilvania din Brașov |
| Series/Report no.: | 2/2015; |
| Abstract: | Hereditary spherocytosis is the most frequent type of chronic haemolytic anaemia, usually inherited
in an autosomal dominant pattern. We present in this paper a case report of a child diagnosed with hereditary
spherocytosis in the neonatal period. The diagnosis was made in the context of suggestive family history and
typical presentation. The clinical course was outlined by numerous haemolytic crises which required
repeated blood transfusions. |
| Description: | Jurnal Medical Brașovean.2015,nr.2,p.123-125.ISSN 1841-0782,e-ISSN 2247-4706 |
| URI: | http://hdl.handle.net/123456789/2410 |
| ISSN: | 1841-0782 e-ISSN 2247-4706 |
| Appears in Collections: | Jurnal Medical Brașovean - ARHIVA
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