Phenotypic variation in ophthalmic manifestations of MIDAS syndrome (microphthalmia, dermal aplasia, and sclerocornea)

Arch Ophthalmol. 2004 Jul;122(7):1070-4. doi: 10.1001/archopht.122.7.1070.
No abstract available

Publication types

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

MeSH terms

  • Chromosome Deletion*
  • Chromosomes, Human, X / genetics*
  • Corneal Diseases / diagnosis
  • Corneal Diseases / genetics*
  • Diseases in Twins*
  • Ectodermal Dysplasia / diagnosis
  • Ectodermal Dysplasia / genetics*
  • Female
  • Humans
  • Infant, Newborn
  • Male
  • Microphthalmos / diagnosis
  • Microphthalmos / genetics*
  • Phenotype
  • Scleral Diseases / diagnosis
  • Scleral Diseases / genetics*
  • Syndrome