Schimke Immunoosseous Dysplasia associated with undifferentiated carcinoma and a novel SMARCAL1 mutation in a child

Pediatr Blood Cancer. 2013 Sep;60(9):E88-90. doi: 10.1002/pbc.24542. Epub 2013 Apr 29.

Abstract

Schimke Immunoosseous Dysplasia (SIOD) is a rare, autosomal recessive disorder of childhood with classical features of spondyloepiphyseal dysplasia, renal failure, and T cell immunodeficiency. SIOD has been associated with several malignancies, including non-Hodgkin lymphoma and osteosarcoma. About half of SIOD patients have biallelic mutations in SMARCAL1 (SWI/SNF-related matrix-associated actin-dependent regulator of chromatin, subfamily a-like 1). This gene encodes an annealing helicase and replication stress response protein that localizes to damage-stalled DNA replication forks. We report a child with SIOD and a novel S859P missense mutation in SMARCAL1 who developed undifferentiated carcinoma of the sinus.

Keywords: DNA damage response; SMARCAL1; Schimke immunoosseous dysplasia; cancer predisposition syndrome; replication stress response.

Publication types

  • Case Reports
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Substitution
  • Arteriosclerosis / complications
  • Arteriosclerosis / genetics*
  • Carcinoma / genetics*
  • Child, Preschool
  • DNA Helicases / genetics*
  • Humans
  • Immunologic Deficiency Syndromes / complications
  • Immunologic Deficiency Syndromes / genetics*
  • Male
  • Mutation, Missense*
  • Nephrotic Syndrome / complications
  • Nephrotic Syndrome / genetics*
  • Nose Neoplasms / genetics*
  • Osteochondrodysplasias / complications
  • Osteochondrodysplasias / genetics*
  • Primary Immunodeficiency Diseases
  • Pulmonary Embolism / complications
  • Pulmonary Embolism / genetics*

Substances

  • SMARCAL1 protein, human
  • DNA Helicases

Supplementary concepts

  • Schimke immunoosseous dysplasia