MIDAS syndrome respectively MLS syndrome: a separate entity rather than a particular lyonization pattern of the gene causing Goltz syndrome

Am J Med Genet. 1995 May 22;57(1):117-8. doi: 10.1002/ajmg.1320570123.
No abstract available

Publication types

  • Case Reports
  • Comment
  • Letter

MeSH terms

  • Adult
  • Child, Preschool
  • Corneal Diseases / classification*
  • Corneal Diseases / genetics
  • Eye Abnormalities / classification*
  • Eye Abnormalities / genetics
  • Female
  • Focal Dermal Hypoplasia / classification*
  • Focal Dermal Hypoplasia / genetics
  • Humans
  • Skin Abnormalities*
  • Skin Diseases / classification*
  • Skin Diseases / genetics
  • Syndrome
  • X Chromosome