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- Hereditary hemorrhagic telangiectasia - Symptoms and causes
Overview Hereditary hemorrhagic telangiectasia (tuh-lan-jee-uk-TAY-zhuh) is a condition that's passed through families, called inherited It causes atypical links between arteries and veins called arteriovenous malformations (AVMs) The most common sites AVMs affect are the skin, nose, digestive system, lungs, brain and liver
- Hereditary hemorrhagic telangiectasia - Mayo Clinic
Living with hereditary hemorrhagic telangiectasia? Connect with others like you for support and answers to your questions in the Blood Cancers Disorders support group on Mayo Clinic Connect, a patient community
- Understanding Parsonage-Turner syndrome and hereditary brachial plexus . . .
The article provides updated information about PTS and its genetic counterpart, hereditary brachial plexus neuropathy (HBPN) Although the cause or trigger for these attacks is still unclear, some associations, including prior viral infection, surgeries, trauma, vaccination and childbirth, have been identified
- Genetic testing - Mayo Clinic
Carrier testing You might choose to have genetic testing before having children if there is a history of an inherited condition or if you want to know your risk of certain hereditary diseases This testing can show if you carry certain gene changes and could pass on a condition to your children
- Alzheimers genes: Are you at risk? - Mayo Clinic
Researchers have found several genes that are linked to Alzheimer's disease Some genes, called risk genes, increase the likelihood of getting the disease Others, called deterministic genes, cause the disease Deterministic genes are rare Genes are only part of what's involved in getting Alzheimer's disease
- Amyloidosis - Symptoms and causes - Mayo Clinic
Hereditary ATTR amyloidosis, also called familial transthyretin amyloidosis This inherited condition often affects the nerves, heart and kidneys It most commonly happens with changes to the TTR protein made by your liver This altered protein is passed down through families Other hereditary forms of amyloidosis
- Charcot-Marie-Tooth disease - Symptoms causes - Mayo Clinic
Risk factors Charcot-Marie-Tooth disease is a hereditary disease That means it passes from parents to children through genes The risk of getting the condition is higher for people who have parents or brothers or sisters with the condition
- Amyotrophic lateral sclerosis (ALS) - Symptoms and causes
Overview Amyotrophic lateral sclerosis (a-my-o-TROE-fik LAT-ur-ul skluh-ROE-sis) is a nervous system disease that affects nerve cells in the brain and spinal cord Also known as ALS, the disease leads to muscle weakness and gets worse over time ALS often begins with muscle twitching and weakness in an arm or leg, trouble swallowing, or slurred speech Eventually ALS affects the muscles needed
- Factor V Leiden - Diagnosis and treatment - Mayo Clinic
Diagnosis Your doctor may suspect factor V Leiden if you've had one or more episodes of abnormal blood clotting or if you have a strong family history of abnormal blood clots Your doctor can confirm that you have factor V Leiden with a blood test
- Ataxia - Symptoms and causes - Mayo Clinic
Hereditary causes Some types of ataxia and some conditions that cause ataxia are passed down in families These conditions also are called hereditary If you have one of these conditions, you may have been born with a genetic change that causes the body to make irregular proteins
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