Early diagnosis of Schöpf-Schulz-Passarge syndrome by whole-exome sequencing: the first Chinese case

J Eur Acad Dermatol Venereol. 2022 Sep;36(9):e722-e724. doi: 10.1111/jdv.18228. Epub 2022 May 28.
No abstract available

Publication types

  • Letter

MeSH terms

  • Anodontia
  • China
  • Early Diagnosis
  • Eccrine Glands / abnormalities
  • Exome Sequencing
  • Eyelid Neoplasms
  • Humans
  • Hypotrichosis* / diagnosis
  • Hypotrichosis* / genetics
  • Keratoderma, Palmoplantar
  • Mutation
  • Pedigree

Supplementary concepts

  • Schopf-Schulz-Passarge Syndrome