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What is a genetically linked disease?
A genetically linked disease is a condition that has a known genetic basis, meaning that it is caused by mutations in specific genes or variations in the DNA sequence. These mutations can be inherited from one or both parents and can increase the risk of developing the disease. Examples include cystic fibrosis, Huntington's disease, and sickle cell anemia.
What is it called when you have only one dominant allele to get the disease?
if an indivigual has a dominent allele for a disease he/she is an affected individual.
What is the salt of seizunil syrup?
Seizunil syrup, also known as sodium valproate syrup, comes in a salt form called sodium valproate. Sodium valproate is a medication used to treat seizures and bipolar disorder by stabilizing electrical activity in the brain.
What is the genetic risk of hypospadias?
The genetic risk of hypospadias is estimated to be around 7-10%, suggesting a multifactorial etiology involving both genetic and environmental factors. Studies have shown an increased incidence of hypospadias among first-degree relatives of affected individuals, indicating a potential genetic component to the condition.
What is An example of a genetic disorder that is both genetic and congenital?
An example of a genetic disorder that is both genetic and congenital is Down syndrome, also known as trisomy 21. It is caused by the presence of an extra copy of chromosome 21, which occurs at conception. This condition is present at birth and is associated with various physical and developmental challenges. Other examples include cystic fibrosis and sickle cell disease, which also arise from genetic mutations and manifest at birth.
Is leprosy a genetic disease?
Known as Hansen's Disease, it is not genetic, but caused by an organism.
What kind of harm can taking medications for bipolar disease effect a fetus?
Several bipolar medications are known to cause birth defects.
What are the characteristics of a genetic disease?
A genetic disease is a disease that was either passed onto you and/or your family is known to get that disease. An example of a genetic disease would be CF (Cystic Fibrosis). It occurs when a cell changes it's genetic information.
What is bipolar and how would you know if you had it?
You can tell if you have bipolar disease by going to the doctor and getting some tests done. The doctor will be able to determine if you indeed do have bipolar disease. You cannot diagnose yourself with something like this.
When was bipolar disorder first labeled?
The disease was known since ancient times, but was first classified by Emil Kraepelin in the 1880s and 1890s.
What mutation causes bipolar disorder?
Bipolar means you have mixed emotions. For example, you can be super happy at one moment and then later you can feel depressed. Being bipolar isn't bad but, its better not to be.An international team of scientists, led by researchers at the University of California, San Diego School of Medicine, reports that abnormal sequences of DNA known as rare copy number variants, or CNVs, appear to play a significant role in the risk for early onset bipolar disorder.The findings will be published in the December 22 issue of the journal Neuron.CNVs are genomic alterations in which there are too few or too many copies of sections of DNA. Researchers have known that spontaneously occurring (de novo) CNVs - genetic mutations not inherited from parents - significantly increase the risk for some neuropsychiatric conditions, such as schizophrenia or the autism spectrum disorders. But their role was unclear in bipolar disorder, previously known as manic depression.Principal investigator Jonathan Sebat, PhD, assistant professor of psychiatry and cellular and molecular medicine at UC San Diego's Institute of Genomic Medicine, and colleagues, found thatde novo CNVs contribute significant genetic risk in about 5 percent of early onset bipolar disorder, which appears in childhood or early adulthood.In other words, said the study's first author Dheeraj Malhotra, assistant project scientist in Sebat's lab, "having a de novo mutation increases the chances of having an earlier onset of disease."The cause or causes of bipolar disorder remain unclear. There is a clear genetic component - the disease runs in families - but previous studies that have focused mainly on common inherited variants have met with limited success in identifying key susceptibility genes.
What is bipolar ic?
ic made from bjt is known as bipolar ic
Is Parkinsons a genetic disease?
Most people with Parkinson's disease have idiopathic Parkinson's disease (having no specific known cause). A small proportion of cases, however, can be attributed to known genetic factors. Other factors have been associated with the risk of developing PD, but no causal relationship has been proven.PD traditionally has been considered a non-genetic disorder; however, around 15% of individuals with PD have a first-degree relative who has the disease. At least 5% of people are now known to have forms of the disease that occur due to a mutation of one of several specific genes.Read more: parkinson-s-disease
Can acupressure be a treatment for bipolar disorder?
It's not known to be an effective treatment for bipolar disorder.
Is Bipolar disorder genetic?
Yes BiPolar is genetic and it is highly likely that someone who has BiPolar has a family member with the same condition. But not always i mean someone has to be first.
What was bi-polar once known as?
The disorder known as bipolar was once known as manic depression. The disorder was changed to bipolar because the disorders were too similar to be known as two separate conditions.
A disorder caused partly or completely by a defect in genes?
There are dozens of diseases caused by a genetic defect. They are known as genetic diseases. Sickle Cell anemia, Hemophilia, Tay-Sachs, Huntingtons Disease- and many others are genetic diseases.
