📂 Diseases
Bardet-Biedl syndrome — Definition
Bardet-Biedl sendromu / Bardet-Biedl syndrome
Bardet-Biedl syndrome is a rare genetic disease, showing autozomal resessive transition. The main findings include retinal dystrophy-related vision loss, obesity, polyminite (gold fingeriness), kidney anomalies and learning strength. The disease is caused by defects in primary silia structure, and therefore it is classified in the group of silipatis. Diagnosis, clinical criteria and genetic tests, treatment requires symptomatic and multidisciplinary approach.
Frequently Asked Questions
❓ What is Bardet-Biedl sendromu?
Bardet-Biedl sendromu; bardet-Biedl syndrome is a rare genetic disease, showing autozomal resessive transition. The main findings include retinal dystrophy-related vision loss, obesity, polyminite (gold fingeriness), kidney anomalies and learning strength. The disease is caused by defects in primary silia structure, and therefore it is classified in the group of silipatis. Diagnosis, clinical criteria and genetic tests, treatment requires symptomatic and multidisciplinary approach.
❓ What is Bardet-Biedl syndrome in Turkish?
The Turkish equivalent of "Bardet-Biedl syndrome" is Bardet-Biedl sendromu.
❓ Which medical field is Bardet-Biedl sendromu related to?
This term belongs to the Diseases category.