A case report of rare ZC4H2-associated disorders associated with three large hernias

Pediatr Int. 2020 Aug;62(8):985-986. doi: 10.1111/ped.14211. Epub 2020 Jul 20.
No abstract available

Keywords: Spigelian hernia; ZC4H2 gene; inguinal hernia; paraesophageal hiatal hernia; rare ZC4H2-associated disorder.

Publication types

  • Case Reports

MeSH terms

  • Apraxias / complications*
  • Apraxias / genetics
  • Contracture / complications*
  • Contracture / genetics
  • Exome Sequencing
  • Fatal Outcome
  • Genetic Diseases, X-Linked / complications*
  • Genetic Diseases, X-Linked / genetics
  • Hernia / complications*
  • Hernia, Hiatal / complications
  • Hernia, Inguinal / complications
  • Hernia, Ventral / complications
  • Humans
  • Infant
  • Intestinal Pseudo-Obstruction / complications
  • Intracellular Signaling Peptides and Proteins / genetics*
  • Male
  • Muscular Atrophy / complications*
  • Muscular Atrophy / genetics
  • Mutation
  • Nuclear Proteins / genetics*
  • Ophthalmoplegia / complications*
  • Ophthalmoplegia / genetics
  • Pneumonia, Aspiration / complications

Substances

  • Intracellular Signaling Peptides and Proteins
  • Nuclear Proteins
  • ZC4H2 protein, human

Supplementary concepts

  • Wieacker syndrome