Neonatal hyperinsulinemic hypoglycemia in a patient with 9p deletion syndrome

Eur J Med Genet. 2018 Aug;61(8):473-477. doi: 10.1016/j.ejmg.2018.03.009. Epub 2018 Mar 27.

Abstract

We report the clinical and neuroradiological findings in a young boy harboring the 9p deletion syndrome including the novel findings of thalamic infarction and germinal matrix haemorrhage and neonatal hyperinsulinemic hypoglycemia. Both the hypoglycemic events and the ventriculomegaly found in this patient have previously only been reported in two patients, while the thalamic infarction and germinal matrix haemorrhage are novel features.

Keywords: 9p deletion syndrome; Craniofacial abnormality; Craniosynostosis; Germinal matrix haemorrhage; Neonatal hyperinsulinemic hypoglycemia; Thalamic infarction; Ventriculomegaly.

Publication types

  • Case Reports

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Abnormalities, Multiple / pathology
  • Chromosome Deletion
  • Chromosome Disorders / genetics*
  • Chromosome Disorders / pathology
  • Chromosomes, Human, Pair 9 / genetics
  • Humans
  • Hyperinsulinism / genetics*
  • Hyperinsulinism / pathology
  • Hypoglycemia / genetics*
  • Hypoglycemia / pathology
  • Infant
  • Male

Supplementary concepts

  • Chromosome 9p Deletion Syndrome