Homozygous deletion in CDH3 and hypotrichosis with juvenile macular dystrophy

Arch Ophthalmol. 2012 Nov;130(11):1490-2. doi: 10.1001/archophthalmol.2012.708.
No abstract available

Publication types

  • Case Reports
  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Sequence
  • Cadherins / genetics*
  • DNA / genetics*
  • DNA Mutational Analysis
  • Diagnosis, Differential
  • Homozygote
  • Humans
  • Hypotrichosis / complications
  • Hypotrichosis / diagnosis
  • Hypotrichosis / genetics*
  • Macular Degeneration / complications
  • Macular Degeneration / diagnosis
  • Macular Degeneration / genetics*
  • Male
  • Middle Aged
  • Mutation*
  • Sequence Deletion*

Substances

  • CDH3 protein, human
  • Cadherins
  • DNA