Myeloid dysplasia in familial 3-methylglutaconic aciduria

J Pediatr Hematol Oncol. 2006 Feb;28(2):69-72. doi: 10.1097/01.mph.0000199585.98926.55.

Abstract

A kindred is reported with four members affected with neurodegenerative disorder and 3-methylglutaconic aciduria. Two siblings developed thrombocytopenia heralding a myelodysplastic syndrome; in one patient it evolved into acute myeloid leukemia with monosomy 7 in the marrow. The hematologic complications have hitherto not been previously reported in other cases of 3-methylglutaconic aciduria and are thus thought to represent a new disease entity. This family adds additional evidence to the genetic heterogeneity of Mendelian disorders in which the primary mutation may have a mutator effect that could give origin to myelodysplastic syndrome and acute myeloid leukemia through acquired chromosomal changes.

Publication types

  • Case Reports

MeSH terms

  • Child, Preschool
  • Chromosomes, Human, Pair 7 / genetics
  • Consanguinity
  • Ethnicity / genetics
  • Female
  • Glutarates / urine*
  • Humans
  • Infant
  • Intellectual Disability / genetics
  • Israel
  • Leukemia, Myeloid, Acute / genetics
  • Male
  • Metabolism, Inborn Errors / complications*
  • Metabolism, Inborn Errors / urine
  • Monosomy
  • Myelodysplastic Syndromes / genetics*
  • Pedigree
  • Thrombocytopenia / genetics

Substances

  • Glutarates
  • 3-methylglutaconic acid