DCN gene related symptoms and diseases
All the information presented here about the DCN gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: HGNC,NCBIGENE,OMIM,ORPHANET, Mendelian Rare Disease Search Engine.
Top 5 symptoms and clinical features associated to DCN gene
Symptoms // Phenotype | % Cases |
---|---|
Nystagmus | Very Common - Between 80% and 100% cases |
Strabismus | Very Common - Between 80% and 100% cases |
Glaucoma | Very Common - Between 80% and 100% cases |
Photophobia | Very Common - Between 80% and 100% cases |
Abnormality of the eye | Very Common - Between 80% and 100% cases |
Other less frequent symptoms and clinical features
Patients with DCN gene alterations may also develop some of the following symptoms and phenotypes:Commonly - More than 50% cases
- Corneal opacity
- Esotropia
- Progressive visual loss
- Exotropia
- Corneal dystrophy
- Congenital glaucoma
- Congenital corneal dystrophy
- Increased corneal thickness
Rare diseases associated to DCN gene
Here you will find a list of rare diseases related to the DCN. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
CONGENITAL STROMAL CORNEAL DYSTROPHY
Alternate names
CONGENITAL STROMAL CORNEAL DYSTROPHY Is also known as congenital stromal corneal dystrophy, cscd, witschel dystrophy, congenital hereditary stromal dystrophy
Description
Congenital stromal corneal dystrophy (CSCD) is an extremely rare form of stromal corneal dystrophy (see this term) characterized by opaque flaky or feathery clouding of the corneal stroma, and moderate to severe visual loss.
Most common symptoms of CONGENITAL STROMAL CORNEAL DYSTROPHY
- Nystagmus
- Strabismus
- Glaucoma
- Photophobia
- Abnormality of the eye
More info about CONGENITAL STROMAL CORNEAL DYSTROPHY
Search interest in DCN
Potential gene panels for DCN gene
DCN Panel
By Institute for Human Genetics University Clinic Freiburg
This panel specifically test the DCN gene.
More info about this panelCorneal Dystrophies Sequencing Panel with CNV Detection Panel
By PreventionGenetics PreventionGenetics Corneal Dystrophies Sequencing Panel with CNV Detection that also includes the following genes: TACSTD2 TCF4 ZEB1 TGFBI VSX1 OVOL2 SLC4A11 COL8A2 CYP4V2 ZNF469
More info about this panelEye Diseases - panels Panel
By MGZ Medical Genetics Center Eye Diseases - panels that also includes the following genes: BFSP1 BFSP2 SALL2 BMP4 BMP7 SHH SIX3 SIX6 FOXL2 SOX2
More info about this panelCongenital Stromal Corneal Dystrophy Panel
By Bioscientia GmbH Center for Human Genetics
This panel specifically test the DCN gene.
More info about this panelCorneal Dystrophy Panel
By Asper Biogene Asper Biogene LLC Corneal Dystrophy that also includes the following genes: SOD1 TACSTD2 TCF4 ZEB1 TGFBI VSX1 SLC4A11 COL17A1 COL8A2 CYP4V2
More info about this panelEye diseases comprehensive panel Panel
By Asper Biogene Asper Biogene LLC Eye diseases comprehensive panel that also includes the following genes: RGS9 RHO GRK1 RLBP1 ROM1 RP1 RP2 RP9 RPE65 RPGR
More info about this panelDCN Panel
By Fulgent Genetics Fulgent Genetics
This panel specifically test the DCN gene.
More info about this panelCorneal Dystrophy Panel Panel
By Blueprint Genetics Corneal Dystrophy Panel that also includes the following genes: TACSTD2 TCF4 ZEB1 TGFBI OVOL2 SLC4A11 COL17A1 COL5A1 COL8A2 CYP4V2
More info about this panelCorneal Dystrophy , Panel Massive Sequencing (NGS) 18 Genes Panel
By Reference Laboratory Genetics Corneal Dystrophy , Panel Massive Sequencing (NGS) 18 Genes that also includes the following genes: TACSTD2 TCF4 ZEB1 TGFBI VSX1 SLC4A11 COL5A1 COL8A2 CYP4V2 ZNF469
More info about this panelIf you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like KCND2