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Acromicric dysplasia with stiff skin syndrome-like severe cutaneous presentation in an 8-year-old boy with a missense FBN1 mutation: Case report and literature review.

Wang TaoYuyan YangQi DongHuijuan ZhuYuehua Liu
Published in: Molecular genetics & genomic medicine (2020)
This is a report about acromicric dysplasia with stiff skin syndrome-like severe cutaneous presentation caused by a single hotspot mutation, further revealing the gene pleiotropy of FBN1.
Keyphrases
  • case report
  • soft tissue
  • early onset
  • wound healing
  • genome wide
  • intellectual disability
  • copy number
  • gene expression
  • dna methylation