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Scapula alata as presenting symptom of Fanconi anemia: A case for serendipity.

Renee van AdrichemVincent de WegerDaniel BroereFemke van HerrewegenJeremy AmayaGavin William Ten Tusscher
Published in: Clinical case reports (2019)
Fanconi anemia is a recessive genetic disorder with a wide range of presenting symptoms, from multiple congenital defects to exclusively (pan) cytopenia. Scapula alata may be a rare symptom of FA.
Keyphrases
  • iron deficiency
  • chronic kidney disease
  • case report
  • patient reported
  • intellectual disability
  • copy number
  • sleep quality
  • muscular dystrophy
  • dna methylation