Phakomatoses

(a.k.a. Systemic Harmatomatoses)

• Tuberous Sclerosis Complex
• Neurofibromatosis Type 1
• Neurofibromatosis Type 2
• Von Hippel-Lindeau Syndrome (Retinocerebellar Hemangiomatosis)
• Sturge-Weber Syndrome (Encephalofacial Hemangiomatosis)
• Phakomatosis Pigmentovascularis
• Wyburn-Mason Syndrome (Racemose Hemangiomatosis)
• Retinal Cavernous Hemangiomatosis with Cutaneous and Central Nervous System Vascular Malformations
• Organoid Nevus Syndrome
• Others that some classify as phakomatoses
  • Louis-Bar Syndrome (Ataxia telangiectasia)
  • Oculodermal melanocytosis
  • Kippel-Trenaunay-Weber syndrome
  • Diffuse Neonatal Hemangiomatosis