STRADA gene related symptoms and diseases
All the information presented here about the STRADA gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: OMIM,HGNC,NCBIGENE,ORPHANET, Mendelian Rare Disease Search Engine.
Top 5 symptoms and clinical features associated to STRADA gene
Symptoms // Phenotype | % Cases |
---|---|
Intellectual disability | Very Common - Between 80% and 100% cases |
Tented upper lip vermilion | Very Common - Between 80% and 100% cases |
Focal-onset seizure | Very Common - Between 80% and 100% cases |
Status epilepticus | Very Common - Between 80% and 100% cases |
Thick lower lip vermilion | Very Common - Between 80% and 100% cases |
Other less frequent symptoms and clinical features
Patients with STRADA gene alterations may also develop some of the following symptoms and phenotypes:Commonly - More than 50% cases
- Open mouth
- Narrow face
- Increased body weight
- Nephrocalcinosis
- Shock
- Drooling
- Focal impaired awareness seizure
- Highly arched eyebrow
And 36 more phenotypes, you can get all of them using our tools for rare diseases.
Rare diseases associated to STRADA gene
Here you will find a list of rare diseases related to the STRADA. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
POLYHYDRAMNIOS-MEGALENCEPHALY-SYMPTOMATIC EPILEPSY SYNDROME
Alternate names
POLYHYDRAMNIOS-MEGALENCEPHALY-SYMPTOMATIC EPILEPSY SYNDROME Is also known as pmse syndrome
Most common symptoms of POLYHYDRAMNIOS-MEGALENCEPHALY-SYMPTOMATIC EPILEPSY SYNDROME
- Intellectual disability
- Seizures
- Global developmental delay
- Generalized hypotonia
- Hypertelorism
More info about POLYHYDRAMNIOS-MEGALENCEPHALY-SYMPTOMATIC EPILEPSY SYNDROME
Search interest in STRADA
Potential gene panels for STRADA gene
Epilepsy and Seizure Plus Sequencing Panel with CNV Detection Panel
By PreventionGenetics PreventionGenetics Epilepsy and Seizure Plus Sequencing Panel with CNV Detection that also includes the following genes: RORB RYR3 SCN1A SCN1B SCN2A SCN3A SCN5A SCN8A SCN9A SGCE
More info about this panelMental Retardation and Dysmorphology - panels Panel
By MGZ Medical Genetics Center Mental Retardation and Dysmorphology - panels that also includes the following genes: RIT1 ROR2 RPL10 RPS6KA3 RRAS SALL1 SF3B4 SGSH ST3GAL3 SLC16A2
More info about this panelSyndromal Diseases - panels Panel
By MGZ Medical Genetics Center Syndromal Diseases - panels that also includes the following genes: RIT1 ROR2 RPL10 RPS6KA3 RRAS SALL1 SF3B4 SGSH ST3GAL3 SLC16A2
More info about this panelAllNeuro panel Panel
By Centogene AG - the Rare Disease Company AllNeuro panel that also includes the following genes: BCS1L ROR2 RPL10 BDNF RPS6KA3 RTN2 RYR1 SACS BIN1 SBF1
More info about this panelSTRADA Panel
By Fulgent Genetics Fulgent Genetics
This panel specifically test the STRADA gene.
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 GCKR FANCL ABCD4 PITX1 MLYCD CFHR1 LEPR