Gunal-Seber-Basaran syndrome

Gunal-Seber-Basaran syndrome is an exceedingly rare presentation of multiple bone islands, i.e. osteopoikilosis. It is characterized by dacryocystitis due to lacrimal canal stenosis with osteopoikilosis ^1-3. This syndrome has an autosomal dominant inheritance ^2,3.

History and etymology

The combination of dacryocystitis with osteopoikilosis was first described in 1993 by three Turkish clinicians, two orthopedic surgeons, lzge Günal​ and S Seber, and a medical geneticist N Basaran ².

See also

• osteopoikilosis
• dermatofibrosis lenticularis disseminata with osteopoikilosis