[Molecular biology as a diagnostic tool in the newborn Emergency department: a rare case of idiopathic infantile arterial calcification]

G Ital Cardiol (Rome). 2016 Mar;17(3):234-6. doi: 10.1714/2190.23670.
[Article in Italian]

Abstract

A Turkish female infant of 96 days was admitted to the pediatric emergency room because of inconsolable crying, persistent cough, and difficulty in feeding during the previous day. She was conscious and did not show any signs or symptoms of multiorgan failure. A few minutes afterwards, the child experienced cardiac arrest with an initial cardiac rhythm of asystole and died 75 minutes later following cardiopulmonary resuscitation maneuvers. As the pathological cause of death, autopsy findings revealed a rare type of idiopathic infantile arterial calcification resulting from a mutation in the gene encoding for the ENPP1 enzyme.

Publication types

  • Case Reports
  • English Abstract

MeSH terms

  • Arteries / pathology
  • Biomarkers / blood
  • Cardiopulmonary Resuscitation / adverse effects*
  • Emergency Service, Hospital*
  • Fatal Outcome
  • Female
  • Heart Arrest / etiology*
  • Humans
  • Infant
  • Mutation*
  • Phosphoric Diester Hydrolases / genetics*
  • Pyrophosphatases / genetics*
  • Rare Diseases
  • Vascular Calcification / complications*
  • Vascular Calcification / diagnosis*
  • Vascular Calcification / genetics

Substances

  • Biomarkers
  • Phosphoric Diester Hydrolases
  • ectonucleotide pyrophosphatase phosphodiesterase 1
  • Pyrophosphatases

Supplementary concepts

  • Arterial calcification of infancy