Publication
Hydrops fetalis associated with erythrocyte pyruvate kinase deficiency
| dc.contributor.author | Ferreira, Paula | |
| dc.contributor.author | Morais, Lurdes | |
| dc.contributor.author | Costa, Ricardo | |
| dc.contributor.author | Resende, C. | |
| dc.contributor.author | Dias, Clara Paz | |
| dc.contributor.author | Araújo, Filomena | |
| dc.contributor.author | Costa, Elísio | |
| dc.contributor.author | Barbot, José | |
| dc.contributor.author | Vilarinho, António | |
| dc.date.accessioned | 2008-02-19T15:11:17Z | |
| dc.date.available | 2008-02-19T15:11:17Z | |
| dc.date.issued | 2000 | |
| dc.description.abstract | The authors report a case of hydrops fetalis due to severe pyruvate kinase deficiency, the most unusual clinical manifestation of this disease. Conclusion Pyruvate kinase deficiency, as other erythrocyte enzymopathies, must be considered in the diferential diagnosis of non-immune hydrops fetalis. This has important implications for clinical investigations, therapy and genetic counselling. | en |
| dc.identifier.citation | Ferreira, Paula; Morais, Lurdes; Costa, Ricardo; Resende, Carlos; Paz Dias, Clara; Araújo, Filomena; Costa, Elísio; Barbot, José; Vilarinho, António (2000). Hydrops fetalis associated with erythrocyte pyruvate kinase deficiency. European Journal of Pediatrics. ISSN 0340-6199. 159:7, p. 481-482 | en |
| dc.identifier.issn | 0340-6199 | |
| dc.identifier.uri | http://hdl.handle.net/10198/495 | |
| dc.language.iso | eng | en |
| dc.publisher | Springer | en |
| dc.subject | Pyruvate kinase | en |
| dc.subject | Hydrops fetalis | en |
| dc.subject | Haemolytic anaemia | en |
| dc.subject | Mutations | en |
| dc.title | Hydrops fetalis associated with erythrocyte pyruvate kinase deficiency | en |
| dc.type | journal article | |
| dspace.entity.type | Publication | |
| rcaap.rights | openAccess | |
| rcaap.type | article | en |