Fumarase deficiency: a rare disorder on the crossroads of clinical and metabolic genetics, neurology and cancer

Clin Dysmorphol. 2017 Apr;26(2):117-120. doi: 10.1097/MCD.0000000000000148.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Alleles
  • Child, Preschool
  • Echocardiography
  • Energy Metabolism / genetics
  • Exome Sequencing
  • Female
  • Fumarate Hydratase / deficiency*
  • Genotype
  • Humans
  • In Situ Hybridization, Fluorescence
  • Karyotype
  • Magnetic Resonance Imaging
  • Metabolism, Inborn Errors / diagnosis*
  • Metabolism, Inborn Errors / etiology*
  • Muscle Hypotonia / diagnosis*
  • Muscle Hypotonia / etiology*
  • Pedigree
  • Phenotype
  • Psychomotor Disorders / diagnosis*
  • Psychomotor Disorders / etiology*
  • Symptom Assessment

Substances

  • Fumarate Hydratase

Supplementary concepts

  • Fumaric aciduria