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Are there any celebs with stickler syndrome?
Yes, actress Bella Thorne has been open about her diagnosis of Stickler syndrome. Stickler syndrome is a rare genetic disorder that affects connective tissues in the body, leading to various symptoms such as joint problems, vision issues, and facial features characteristic of the syndrome.
Is the ability to identify the bones of the body an inherited trait?
No, knowing the names and locations of bones is an aspect of knowledge, something gained through learning. You cannot inherently identify bones because knowledge is not a trait. However, the capacity to learn to identify bones is an inherited trait.
Is marfan syndrome a genetic disease?
Yes, Marfan syndrome is a genetic disorder. It is not a disease. It is caused by a mutation in fibrillin and is an autosomal dominant mutation. This means that if you have a Marfan causing mutation, you have Marfan, and you have a 50/50 chance of passing it on to any children you may have. Severity of Marfan can vary within a family, even though all affected family members have the same mutation. It can not skip generations.
What is werewolf syndrome?
"Werewolf Syndrome" has been classified as lycanthropy. Lycanthropy is the disease in which you believe you are turning into a wild animal, although physical symptoms are not present. there is also a different definition to werewolf syndrome, in which the person has a genetic defect/ mutation. this mutation is rare and this is all it really means: instead of the person only growing hair on their head, they also grow it on their face and possibly arms/legs. this is not to be confused with normal body hair. the hair actually is quite similar to the hair on an average person's head. These people, other than their appearance, are completely normal.
What is the genetic cause of Marfan syndrome?
Marfan syndrome is a disorder of the connective tissue. Connective tissue provides strength and flexibility to structures throughout the body such as bones, ligaments, muscles, the walls of blood vessels, and heart valves. It is caused by a mutation in fibrillin, which decreases fibrillin production and increases TGF-B production. 90-95% of people with Marfan syndrome are able to identify their mutation on FBN1. The other 5-10% may have a mutation on another gene that affects the production of fibrillin which we have not yet discovered. Marfan syndrome affects most organs and tissues, especially the skeleton, lungs, eyes, heart, and the large blood vessel that distributes blood from the heart to the rest of the body (the aorta). The signs and symptoms of Marfan syndrome vary widely in severity, timing of onset, and rate of progression. Affected individuals often are tall (as compared to unaffected family members) and slender, have elongated fingers and toes (arachnodactyly), and have an arm span that exceeds their body height. Other common features include unusually flexible joints, a long and narrow face, a highly arched roof of the mouth, crowded teeth, an abnormal curvature of the spine (scoliosis), and either a sunken chest (pectus excavatum) or a protruding chest (pectus carinatum). About half of all people with Marfan syndrome have vision problems caused by a dislocated lens (ectopia lentis) in one or both eyes, and most have some degree of nearsightedness (myopia). Clouding of the lens (cataract) may occur early on, even in childhood, and increased pressure within the eye (glaucoma) occurs more frequently in people with Marfan syndrome than in those without the condition.
Is marfan syndrome dominant or recessive?
Marfan's Syndrome is inherited in an autosomal dominant pattern. This disease is a disorder that affects the connective tissue in many parts of the body.
What is Marquio syndrome?
Morquio syndrome is an inherited disease of metabolism in which the body is missing or doesn't have enough of a substance needed to break down long chains of sugar molecules called glycosaminoglycans
What is morphan's syndrome?
what is morphan syndromwhat is morphan syndromMarfan syndromeA connective tissue, multisystemic disorder characterized by skeletal changes (arachnodactyly ; long limbs, joint laxity, pectus), cardiovascular defects (aortic aneurysm which may dissect, mitral valve prolapse), and ectopia lentis; autosomal dominant inheritance, caused by mutation in the fibrillin-1 gene (FBN1) on chromosome 15q.
What is the phenotype of marfan syndrome?
Marfan syndrome is characterized by a tall and slender stature, long limbs, and disproportionately long fingers and toes (arachnodactyly). Individuals may also exhibit cardiovascular abnormalities, particularly affecting the aorta, as well as skeletal issues like scoliosis and pectus excavatum. Other features can include eye problems such as lens dislocation and myopia. Overall, the phenotype results from mutations in the fibrillin-1 gene, affecting connective tissue throughout the body.
Where is down syndrome on your body?
Down Syndrome Is In Your Brain.
When was The Body-Hat Syndrome created?
The Body-Hat Syndrome was created on 1993-10-05.
How are finger prints inherited?
They are because most patrs of your body are inherited from your parents.
Is werewolf syndrome genetic?
If you are refering to Hypertrichosis, when the body grows abnormally large amounts of hair, then yes. "Werewolf Syndrome" Is genetic and is thought to be caused by a mutation in one of the chromosomes.
In whales the pelvis and femur are?
body parts inherited from a distant ancestor that have not disapeared yet.
What is the disease were your insides grow but your body doesn't?
Morquio Syndrome. An example of this is in Freak The Mighty and Kevin is only about 2 feet tall and his heart gets too big for his body.
When was Ehlers-Danlos Syndrome identified?
Hello, I see you are asking "What is ehlers danlos syndrome?" Ehlers-Danlos syndrome is a group of inherited disorders that affect your connective tissues — primarily your skin, joints and blood vessel walls. Connective tissue is a complex mixture of proteins and other substances that provide strength and elasticity to the underlying structures in your body. For more information, you can visit this URL - skincarehealthcenter. com/condition/ehlers-danlos-syndrome/c/12004
What happens to the body that has down syndrome?
it turns into you.
