- Diseases
- Brittle cornea syndrome
Brittle cornea syndrome
Name: |
Brittle cornea syndrome
|
Description: |
A rare, hereditary connective tissue disease characterized by severe ocular manifestations due to extreme corneal thinning and fragility with rupture in the absence of significant trauma, often leading to irreversible blindness. Extraocular manifestations comprise deafness, developmental hip dysplasia, and joint hypermobility.
|
ORPHAcode: |
90354
|
Synonyms: |
Ehlers-Danlos syndrome type 6B
|
XREF(s): | |
Analyte(s): | |
Created: |
13 May 2019 - 01:02
|
Changed: |
22 Jun 2023 - 16:14
|
-
Brittle Cornea (2 genes) - UGent
Gene % of coding sequence sufficiently covered to detect heterozygous mutations Copy number variation Comments ZNF469 PRDM5 -
Corneal dystrophy - UGent
Gene % of coding sequence sufficiently covered to detect heterozygous mutations Copy number variation Comments AGBL1 99.99 1 CHRDL1 99.94 1 CHST6 100.00 1 COL17A1 99.98 1 COL3A1 99.87 1 COL5A1 99.99 1 COL8A2 99.94 1 CYP4V2 99.98 1 DCN 99.42 1 GRHL2 100.00 1 GSN 99.93 1 KERA 99.95 1 KRT12 99.92 1 KRT3 99.89 1 LCAT 99.97 1 LOXHD1 99.99 1 NLRP1 95.26 1 NLRP3 100.00 1 OVOL2 100.00 1 PAX6 99.95 1 PIKFYVE 99.81 1 PITX2 99.98 1 PRDM5 99.76 1 SLC4A11 100.00 1 SOD1 99.97 1 STS 99.81 1 TACSTD2 100.00 1 TCF4 98.56 1 TGFBI 99.89 1 UBIAD1 99.98 1 VSX1 99.93 1 ZEB1 100.00 1 ZNF469 100.00 1 -
Ehlers-Danlos syndrome -UGent
Gene % of coding sequence sufficiently covered to detect heterozygous mutations Copy number variation Comments ADAMTS2 100.00 1 AEBP1 100.00 1 B3GALT6 100.00 1 B3GAT3 100.00 1 B4GALT7 100.00 1 C1R 100.00 1 C1S 100.00 1 CHST14 100.00 1 COL12A1 100.00 1 COL1A1 100.00 1 COL1A2 100.00 1 COL3A1 100.00 1 COL5A1 100.00 1 COL5A2 100.00 1 DSE 100.00 1 FKBP14 100.00 1 PLOD1 100.00 1 PRDM5 100.00 1 RIN2 100.00 1 SLC39A13 100.00 1 XYLT1 100.00 1 XYLT2 100.00 1 ZNF469 100.00 1 FLNA 100.00 1 FLNB 100.00 1 TAB2 100.00 1