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Lessons from a pair of siblings with BPAN

Eur J Hum Genet. 2016 Jul;24(7):1080-3. doi: 10.1038/ejhg.2015.242. Epub 2015 Nov 18.

Abstract

Neurodegeneration with brain iron accumulation (NBIA) encompasses a heterogeneous group of inherited progressive neurological diseases. Beta-propeller protein-associated neurodegeneration (BPAN) has been estimated to account for ~7% of all cases of NBIA and has distinctive clinical and brain imaging findings. Heterozygous variants in the WDR45 gene located in Xp11.23 are responsible for BPAN. A clear female predominance supports an X-linked dominant pattern of inheritance with proposed lethality for germline variants in hemizygous males. By whole-exome sequencing, we identified an in-frame deletion in the WDR45 gene (c.161_163delTGG) in the hemizygous state in a 20-year-old man with a history of profound neurocognitive impairment and seizures. His higher functioning 14-year-old sister, also with a history of intellectual disability, was found to carry the same variant in the heterozygous state. Their asymptomatic mother was mosaic for the alteration. From this pair of siblings with BPAN we conclude that: (1) inherited WDR45 variants are possible, albeit rare; (2) hemizygous germline variants in males can be viable, but likely result in a more severe phenotype; (3) for siblings with germline variants, males should be more significantly affected than females; and (4) because gonadal and germline mosaicism are possible and healthy female carriers can be found, parental testing for variants in WDR45 should be considered.

Publication types

  • Case Reports

MeSH terms

  • Adolescent
  • Adult
  • Carrier Proteins / genetics*
  • Chromosomes, Human, X / genetics
  • Exome
  • Female
  • Gene Deletion
  • Genetic Diseases, X-Linked / genetics*
  • Genetic Diseases, X-Linked / pathology
  • Germ-Line Mutation
  • Hemizygote*
  • Heterozygote
  • Humans
  • Iron Metabolism Disorders / diagnostic imaging
  • Iron Metabolism Disorders / genetics*
  • Iron Metabolism Disorders / pathology
  • Male
  • Mosaicism
  • Neuroaxonal Dystrophies / diagnostic imaging
  • Neuroaxonal Dystrophies / genetics*
  • Neuroaxonal Dystrophies / pathology
  • Pedigree
  • Young Adult

Substances

  • Carrier Proteins
  • WDR45 protein, human

Supplementary concepts

  • Neurodegeneration with brain iron accumulation (NBIA)