Bardet-Biedl syndrome
Autozomálně recesivní
A recessive ciliopathy caused by variants in more than 20 genes (most often BBS1 and BBS10) that causes retinal dystrophy, obesity, extra fingers or toes, kidney anomalies and learning difficulties.
Co se diagnózou změní
Diagnosis allows eye, kidney and diabetes surveillance, and setmelanotide is an approved treatment for obesity in Bardet-Biedl syndrome.
Analyzované geny
Známé také jako
BBS
Zahrnuje 22 příbuzných podtypů ↓Skrýt podtypy ↑
- Bardet-Biedl syndrome 1
- Bardet-Biedl syndrome 10
- Bardet-Biedl syndrome 11
- Bardet-Biedl syndrome 12
- Bardet-Biedl syndrome 13
- Bardet-Biedl syndrome 14
- Bardet-Biedl syndrome 15
- Bardet-Biedl syndrome 16
- Bardet-Biedl syndrome 17
- Bardet-Biedl syndrome 18
- Bardet-Biedl syndrome 19
- Bardet-Biedl syndrome 2
- Bardet-Biedl syndrome 20
- bardet-biedl syndrome 21
- Bardet-Biedl syndrome 22
- Bardet-Biedl syndrome 3
- Bardet-Biedl syndrome 4
- Bardet-Biedl syndrome 5
- Bardet-Biedl syndrome 6
- Bardet-Biedl syndrome 7
- Bardet-Biedl syndrome 8
- Bardet-Biedl syndrome 9
