Severe hyperbilirubinemia in a glucose-6-phosphate dehydrogenase-deficient preterm neonate: could prematurity be the main responsible factor?

Abstract:

:We report on a premature infant with glucose-6-phosphate dehydrogenase deficiency and severe hyperbilirubinemia. In this patient, all known potential hemolytic agents were excluded and no findings of hemolysis were observed. The crucial role of prematurity in the pathogenesis of this type of jaundice is discussed.

journal_name

Fetal Diagn Ther

authors

Costa S,De Carolis MP,De Luca D,Savarese I,Romagnoli C

doi

10.1159/000174571

subject

Has Abstract

pub_date

2008-01-01 00:00:00

pages

440-3

issue

4

eissn

1015-3837

issn

1421-9964

pii

000174571

journal_volume

24

pub_type

杂志文章
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    authors: Danzer E,Gerdes M,Bebbington MW,Sutton LN,Melchionni J,Adzick NS,Wilson RD,Johnson MP

    更新日期:2009-01-01 00:00:00

  • Severity of Fetal Brain Abnormalities in Congenital Heart Disease in Relation to the Main Expected Pattern of in utero Brain Blood Supply.

    abstract:OBJECTIVES:We evaluated the hypothesis that in fetuses with congenital heart disease (CHD) there is a correlation between the expected pattern of in utero brain blood supply and the severity of neurodevelopmental impairment. METHODS:A total of 58 fetuses with CHD and 58 controls underwent a Doppler ultrasound and feta...

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    authors: Masoller N,Sanz-Cortés M,Crispi F,Gómez O,Bennasar M,Egaña-Ugrinovic G,Bargalló N,Martínez JM,Gratacós E

    更新日期:2016-01-01 00:00:00

  • Cord Occlusion in Monochorionic Twins with Early Selective Intrauterine Growth Restriction and Abnormal Umbilical Artery Doppler: A Consecutive Series of 90 Cases.

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    authors: Parra-Cordero M,Bennasar M,Martínez JM,Eixarch E,Torres X,Gratacós E

    更新日期:2016-01-01 00:00:00

  • Ontogeny of recurrent hydrocephalus: presentation in three fetuses in one consanguineous family.

    abstract::A consanguineous couple had 3 pregnancies in which prenatally diagnosed hydrocephalus was observed (in 1 female and 2 male fetuses). This case appears to represent an autosomal recessive form of hydrocephalus, given the consanguinity, affected sibs of both genders, and no evidence for intrauterine infection, chromosom...

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    authors: Brady TB,Kramer RL,Qureshi F,Feldman B,Kupsky WJ,Johnson MP,Evans MI

    更新日期:1999-07-01 00:00:00

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    authors: Housley HT,Graf JL,Lipshultz GS,Calvano CJ,Harrison MR,Farmer DL,Jennings RW

    更新日期:2000-09-01 00:00:00

  • Sequential Amniotic Fluid Thyroid Hormone Changes Correlate with Goiter Shrinkage following in utero Thyroxine Therapy.

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    authors: Munoz JL,Kessler AA,Felig P,Curtis J,Evans MI

    更新日期:2016-01-01 00:00:00

  • Noninvasive Sampling of the Intrauterine Environment in Women with Preterm Labor and Intact Membranes.

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    pub_type: 杂志文章,评审

    doi:10.1159/000480232

    authors: Cobo T,Kacerovsky M,Jacobsson B

    更新日期:2018-01-01 00:00:00

  • Criteria for screening and diagnosis of gestational diabetes mellitus in the first trimester of pregnancy.

    abstract:OBJECTIVE:To propose new cutoffs in plasma glucose levels in screening and diagnosis of gestational diabetes mellitus (GDM) in the first trimester of pregnancy. METHODS:A 50-gram oral glucose challenge test (GCT) was performed in 1,716 singleton pregnancies at 6-14 weeks' gestation. In those with a positive GCT, a 100...

    journal_title:Fetal diagnosis and therapy

    pub_type: 杂志文章

    doi:10.1159/000324684

    authors: Plasencia W,Garcia R,Pereira S,Akolekar R,Nicolaides KH

    更新日期:2011-01-01 00:00:00

  • Co-inheritance of β- and δ-thalassemia compromising prenatal screening in a Chinese couple seeking prevention.

    abstract::Although δ-globin gene mutations have no clinical implications, association of β- and δ-thalassemia may lead to misdiagnosis. We describe the case of a Chinese woman who was assumed to have an α-thalassemia heterozygote, but was later shown to have β-thalassemia with a normal amount of HbA(2) caused by the -77 mutatio...

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    pub_type: 杂志文章

    doi:10.1159/000321046

    authors: Li J,Xie XM,Zhou JY,Li DZ

    更新日期:2011-01-01 00:00:00

  • Feasibility of retroviral vector-mediated in utero gene transfer to the fetal rabbit.

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    pub_type: 杂志文章

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    authors: Moreno R,Rosal M,Cabero L,Gratacós E,Aran JM

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  • Fetoscopic endotracheal occlusion for severe isolated diaphragmatic hernia: initial experience from a single clinic in Brazil.

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    authors: Peralta CF,Sbragia L,Bennini JR,de Fátima Assunção Braga A,Sampaio Rousselet M,Machado Rosa IR,Barini R

    更新日期:2011-01-01 00:00:00

  • Which stem cells should be used for transplantation?

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    journal_title:Fetal diagnosis and therapy

    pub_type: 杂志文章,评审

    doi:10.1159/000074252

    authors: Michejda M

    更新日期:2004-01-01 00:00:00

  • Assessment of fetal cardiac function using tissue Doppler techniques.

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    authors: Comas M,Crispi F

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    journal_title:Fetal diagnosis and therapy

    pub_type: 杂志文章

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    authors: Conley BJ,Trounson AO,Mollard R

    更新日期:2004-05-01 00:00:00

  • Single umbilical artery: Does side matter?

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  • Preterm premature rupture of membranes in a patient with the hypermobility type of the Ehlers-Danlos syndrome. A case report.

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    authors: De Vos M,Nuytinck L,Verellen C,De Paepe A

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  • Epinephrine affects hemodynamics of noninnervated normal and all-trans retinoic acid-treated embryonic chick hearts.

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  • Prenatally evolving ectopia cordis with successful surgical treatment.

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  • Brachial Artery Flow Mediated Dilation in the First Trimester to Predict the Occurrence of Hypertensive Disorders during Pregnancy.

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  • Mathematical models for fetal growth: application for biparietal diameter measurement.

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    doi:10.1159/000264339

    authors: Bondagji N,Manning FA,Martel J,Harman CR,Morrison I

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  • Early Intrauterine Transfusion in Fetuses with Severe Anemia Caused by Parvovirus B19 Infection.

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    pub_type: 杂志文章,多中心研究

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    authors: Hellmund A,Geipel A,Berg C,Bald R,Gembruch U

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