PRKCH gene related symptoms and diseases
All the information presented here about the PRKCH gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: NCBIGENE,OMIM,HGNC, Mendelian Rare Disease Search Engine.
Top 5 symptoms and clinical features associated to PRKCH gene
| Symptoms // Phenotype | % Cases |
|---|---|
| Stroke | Very Common - Between 80% and 100% cases |
| Cerebral hemorrhage | Very Common - Between 80% and 100% cases |
Rare diseases associated to PRKCH gene
Here you will find a list of rare diseases related to the PRKCH. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
STROKE, ISCHEMIC
Alternate names
STROKE, ISCHEMIC Is also known as cerebral infarction, cerebrovascular accident
Description
A stroke is an acute neurologic event leading to death of neural tissue of the brain and resulting in loss of motor, sensory and/or cognitive function. It is said to be the third leading cause of death in the United States. Gunel and Lifton (1996) noted that about 20% of strokes are hemorrhagic, resulting in bleeding into the brain. Ischemic strokes, resulting from vascular occlusion, account for the majority of strokes.Bersano et al. (2008) reviewed genetic polymorphisms that have been implicated in the development of stroke. Candidate genes include those involved in hemostasis (see, e.g., F5; {612309}), the renin-angiotensin-aldosterone system (see, e.g., ACE; {106180}), homocysteine (see, e.g., MTHFR; {607093}), and lipoprotein metabolism (see, e.g., APOE; {107741}).See also hemorrhagic stroke, or intracerebral hemorrhage (ICH ).
Most common symptoms of STROKE, ISCHEMIC
- Stroke
- Cerebral hemorrhage
More info about STROKE, ISCHEMIC
SOURCES: OMIM
Search interest in PRKCH
Potential gene panels for PRKCH gene
AllNeuro panel Panel
Germany.
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 panel Germany.
NOONAN, LEOPARD, COSTELLO and CARDIOFACIOCUTANEOUS SYNDROME Panel
Spain.
By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases NOONAN, LEOPARD, COSTELLO and CARDIOFACIOCUTANEOUS SYNDROME that also includes the following genes: RIT1 SHOX BRAF SOS1 SPRY2 SRC CD2AP GAB2 CBL SHOC2
More info about this panel Spain.
PRKCH Panel
United States.
By Fulgent Genetics Fulgent Genetics
This panel specifically test the PRKCH gene.
More info about this panel United States.
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