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

• G. Haberhauer, M. Skoumal: Osteopoikilose. In: Journal for Mineral Metabolism & Musculoskeletal Diseases , Vol. 12, No. 1, 2005, pp. 5-9

Individual evidence

1. ↑ ^{a b} Orphanet Syndrome de dacryocystite-ostéopoecilie
2. ↑ Osteopoikilosis and Dacryocystitis.  In: Online Mendelian Inheritance in Man . (English)
3. ^ 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 .

Web links

• Right diagnosis

This article is about a health issue. It is not used for self-diagnosis and does not replace a diagnosis by a doctor. Please note the information on health issues !