Cristin-resultat-ID: 1971338
Sist endret: 14. januar 2022, 13:17
NVI-rapporteringsår: 2021
Resultat
Vitenskapelig artikkel
2021

Biallelic ANGPT2 loss-of-function causes severe early-onset non-immune hydrops fetalis

Bidragsytere:
  • Marie Falkenberg Smeland
  • Pascal Brouillard
  • Trine Prescott
  • Laurence M. Boon
  • Bodil Hvingel
  • Cecilie Valborg Nordbakken
  • mfl.

Tidsskrift

Journal of Medical Genetics
ISSN 0022-2593
e-ISSN 1468-6244
NVI-nivå 2

Om resultatet

Vitenskapelig artikkel
Publiseringsår: 2021
Publisert online: 2021

Beskrivelse Beskrivelse

Tittel

Biallelic ANGPT2 loss-of-function causes severe early-onset non-immune hydrops fetalis

Sammendrag

Background: Hydrops fetalis, a pathological fluid accumulation in two or more body compartments, is aetiologically heterogeneous. We investigated a consanguineous family with recurrent pregnancy loss due to severe early-onset non-immune hydrops fetalis. Methods and results: Whole exome sequencing in four fetuses with hydrops fetalis revealed that they were homozygous for the angiopoietin-2 (ANGPT2) variant Chr8 (GRCh37/Hg19): 6385085T>C, NM_001147.2:c.557A>G. The substitution introduces a cryptic, exonic splice site predicted to result in loss of 10 nucleotides with subsequent shift in reading frame, leading to a premature stop codon. RNA analysis in the heterozygous parents demonstrated loss of detectable mutant allele, indicative of loss-of-function via nonsense-mediated mRNA decay. Serum ANGPT2 levels were reduced in the parents. In a pregnancy with a healthy, heterozygous child, transiently increased fetal nuchal translucency was noted. Conclusion: Pathogenic heterozygous ANGPT2 missense variants were recently shown to cause autosomal dominant primary lymphoedema. ANGPT2 is a ligand of the TIE1-TIE2 (tyrosine kinase with immunoglobulin-like and epidermal growth factor-like domains 1 and 2) pathway. It is critical to the formation and remodelling of blood and lymphatic vessels and is involved in vessel maintenance. ANGPT2 knockout mice die from generalised lymphatic dysfunction. We show here that a homozygous pathogenic variant causes loss-of-function and results in severe early-onset hydrops fetalis. This is the first report of an autosomal recessive ANGPT2-related disorder in humans.

Bidragsytere

Marie Smeland

Bidragsyterens navn vises på dette resultatet som Marie Falkenberg Smeland
  • Tilknyttet:
    Forfatter
    ved Barne- og ungdomsklinikken ved Universitetssykehuset Nord-Norge HF

Pascal Brouillard

  • Tilknyttet:
    Forfatter
    ved Université catholique de Louvain

Trine Prescott

  • Tilknyttet:
    Forfatter
    ved Medisinsk serviceklinikk ved Sykehuset Telemark HF

Laurence M. Boon

  • Tilknyttet:
    Forfatter
    ved Belgia

Bodil Hvingel

  • Tilknyttet:
    Forfatter
    ved Kirurgi-, kreft- og kvinnehelseklinikken ved Universitetssykehuset Nord-Norge HF
1 - 5 av 9 | Neste | Siste »