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Hht is a condition of gene changes, called genetic, that you get from your parents This gene codes for the huntingtin protein and within the htt gene is a dna sequence known as the cag trinucleotide repeat. It is an autosomal dominant disorder
That means if one of your parents has hht, you have a 50% chance of getting it Mutations in the htt gene are responsible for huntington's disease If you have hht, each of your children has a 50% chance of getting it from you.
The htt gene provides instructions for making a protein called huntingtin
Although the exact function of this protein is unknown, it appears to play an important role in nerve cells (neurons) in the brain and is essential for normal development before birth. Huntington’s disease is a genetic condition that affects the cells in your brain It’s a progressive condition that gets worse over time Common symptoms affect your movement, thoughts and feelings
Symptoms usually start between the ages of 30 and 50 Treatment is available to help you feel more comfortable Hht is a disorder in which some blood vessels do not develop properly A person with hht may form abnormal capillaries or abnormal capillary connections between the arteries and veins
Capillaries are tiny blood vessels that pass blood from arteries to veins.
Htt (huntingtin) is a protein coding gene Among its related pathways are gene expression (transcription) and transcriptional regulation by mecp2. What is juvenile huntington’s disease (jhd) A small but significant percentage of cases involves onset before the age of 20, known as juvenile huntington’s disease.
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