Phacomatosis pigmentovascularis type IIB associated with Sturge-Weber syndrome: a case report and review of the literature

Genet Couns. 2013;24(2):247-50.
No abstract available

Publication types

  • Case Reports
  • Letter
  • Review

MeSH terms

  • Atrophy
  • Child
  • Developmental Disabilities / genetics
  • Female
  • Humans
  • Intellectual Disability / genetics
  • Neurocutaneous Syndromes / diagnosis*
  • Neurocutaneous Syndromes / pathology
  • Neurocutaneous Syndromes / physiopathology
  • Status Epilepticus / genetics
  • Sturge-Weber Syndrome / diagnosis*
  • Sturge-Weber Syndrome / pathology
  • Sturge-Weber Syndrome / physiopathology

Supplementary concepts

  • Phacomatosis pigmentovascularis