Kongenit methaemoglobinaemi: en sjaelden årsag til neonatal cyanose

Birgitte Smith; Ole Axel Pryds; Ernst Christensen; Allan Meldgaard Lund

Kongenit methaemoglobinaemi: en sjaelden årsag til neonatal cyanose

Birgitte Smith, Ole Axel Pryds, Ernst Christensen, Allan Meldgaard Lund

Børne- og Ungeafdelingen

1 Citationer (Scopus)

Abstract

We present a case study of a newborn girl with a reduced erythrocytic nicotinamide adenine dinucleotide (NADH)-dependent methaemoglobin reductase level. Within the first days of life she developed cyanosis due to a methaemoglobin level of 21%. The hyperoxia test was characteristic, with normal increases in blood oxygen tension, whereas the oxygen saturation remained constant at 92%. Over the next months the methaemoglobin level decreased to 10%, and the girl did well without treatment.
Udgivelsesdato: 2008-Aug-11

Bidragets oversatte titel	Congenital methaemoglobinaemia: an infrequent cause of neonatal cyanosis
Originalsprog	Dansk
Tidsskrift	Ugeskr Laeger
Vol/bind	170
Udgave nummer	33
Sider (fra-til)	2460
Status	Udgivet - 2008

Citationsformater

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abstract = "We present a case study of a newborn girl with a reduced erythrocytic nicotinamide adenine dinucleotide (NADH)-dependent methaemoglobin reductase level. Within the first days of life she developed cyanosis due to a methaemoglobin level of 21%. The hyperoxia test was characteristic, with normal increases in blood oxygen tension, whereas the oxygen saturation remained constant at 92%. Over the next months the methaemoglobin level decreased to 10%, and the girl did well without treatment. Udgivelsesdato: 2008-Aug-11",

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TY - JOUR

T1 - Kongenit methaemoglobinaemi: en sjaelden årsag til neonatal cyanose

AU - Smith, Birgitte

AU - Pryds, Ole Axel

AU - Christensen, Ernst

AU - Lund, Allan Meldgaard

PY - 2008

Y1 - 2008

N2 - We present a case study of a newborn girl with a reduced erythrocytic nicotinamide adenine dinucleotide (NADH)-dependent methaemoglobin reductase level. Within the first days of life she developed cyanosis due to a methaemoglobin level of 21%. The hyperoxia test was characteristic, with normal increases in blood oxygen tension, whereas the oxygen saturation remained constant at 92%. Over the next months the methaemoglobin level decreased to 10%, and the girl did well without treatment. Udgivelsesdato: 2008-Aug-11

AB - We present a case study of a newborn girl with a reduced erythrocytic nicotinamide adenine dinucleotide (NADH)-dependent methaemoglobin reductase level. Within the first days of life she developed cyanosis due to a methaemoglobin level of 21%. The hyperoxia test was characteristic, with normal increases in blood oxygen tension, whereas the oxygen saturation remained constant at 92%. Over the next months the methaemoglobin level decreased to 10%, and the girl did well without treatment. Udgivelsesdato: 2008-Aug-11

KW - Cyanosis

KW - Female

KW - Humans

KW - Infant, Newborn

KW - Methemoglobinemia

M3 - Tidsskriftartikel

C2 - 18761834

SN - 1399-4174

VL - 170

SP - 2460

JO - Ugeskr Laeger

JF - Ugeskr Laeger

IS - 33

ER -