Gunal-Seber-Basaran syndrome

Last revised by Subhan Iqbal on 19 Oct 2021

Citation, DOI, disclosures and article data

Citation:

Iqbal S, Bell D, Gunal-Seber-Basaran syndrome. Reference article, Radiopaedia.org (Accessed on 19 Apr 2024) https://doi.org/10.53347/rID-94036

DOI:

https://doi.org/10.53347/rID-94036

Permalink:

https://radiopaedia.org/articles/94036

rID:

94036

Article created:

16 Oct 2021, Subhan Iqbal

Disclosures:

At the time the article was created Subhan Iqbal had no recorded disclosures.

View Subhan Iqbal's current disclosures

Last revised:

19 Oct 2021, Subhan Iqbal

Disclosures:

At the time the article was last revised Subhan Iqbal had no recorded disclosures.

View Subhan Iqbal's current disclosures

Revisions:

4 times, by 2 contributors - see full revision history and disclosures

Systems:

Musculoskeletal

Sections:

Syndromes

Synonyms:

Dacryocystitis-osteopoikilosis 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.