Günal-Seber-Başaran syndrome
Classification according to ICD-10 | |
---|---|
H04.3 | Acute and unspecified inflammation of the tear ducts |
Q78.8 | Other specified osteochondrodysplasias
Osteopoicilia |
ICD-10 online (WHO version 2019) |
The Günal-Seber-Basaran syndrome is a very rare congenital disease with a combination of Dakryozystitis and osteopoikilosis .
Synonyms are: Gunal-Seber-Basaran syndrome; Syndrome de Gunal-Seber-Basaran; Syndrome de dacryocystite-ostéopoïkilose
The name refers to the first authors of the first description from 1993 by the Turkish doctors I. Günal , S. Seber , N. Başaran and colleagues.
distribution
The frequency is given as less than 1 in 1,000,000, inheritance is autosomal dominant .
literature
Individual evidence
- ↑ a b Orphanet Syndrome de dacryocystite-ostéopoecilie
- ↑ Osteopoikilosis and Dacryocystitis. In: Online Mendelian Inheritance in Man . (English)
- ^ I. Günal, S. Seber, N. Başaran, S. Artan, K. Günal, E. Göktürk: Dacryocystitis associated with osteopoikilosis. In: Clinical genetics. Vol. 44, No. 4, October 1993, pp. 211-213, PMID 8261652 .