At high altitude in the Netherlands: secondary erythrocytosis due to HB-Malmo
We describe two patients, a father and a son, presenting with erythrocytosis. Evaluation showed no pulmonal or cardial disorders. Owing to an elevated erythropoietin level after phlebotomy, a physiological secondary polycythaemia was suspected. A haemoglobin electrophoresis showed that our patients have a haemoglobinopathy with high affinity for oxygen, called Hb-Malmö (exon 3: c.294 C>G p.His98Gln). Hb-Malmö is a congenital disorder located on a gene at chromosome 11, in the B-chain on codon 97, decoding the α-subunit and β-subunit of the haemoglobin. Through a mutation (CAC→CAG), histidin... Mehr ...
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Dokumenttyp: | TEXT |
Erscheinungsdatum: | 2014 |
Verlag/Hrsg.: |
BMJ Publishing Group Ltd
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Schlagwörter: | case-report |
Sprache: | Englisch |
Permalink: | https://search.fid-benelux.de/Record/base-29175527 |
Datenquelle: | BASE; Originalkatalog |
Powered By: | BASE |
Link(s) : | http://casereports.bmj.com/cgi/content/short/2014/mar05_1/bcr2014203701 |