Joint hypermobility syndrome (JHS) and Ehlers-Danlos syndrome, hypermobility type (EDS-HT) are the tissue disorders which can be characterized by chronic pain, joint instability complications, and minor skin changes. During these, Fatigue and headache are the very common symptoms; though they can be diagnosed using specific criteria.
JHS/EDS-HT is a rare common condition that could not be diagnosed by most clinicians and pain specialists, resulting in interventions like symptomatic and non-satisfactory treatments, because there is a lack of reasonable pathophysiologic rationale.
Pain, fatigue, and headache in JHS/EDS are usually treated with the help of certain symptoms or on the basis of doctors’ experience.
<span>Therefore, in order to the cure of such symptoms, doctors suggest pathogenic mechanisms. The major aim of the re-writing of the natural history of JHS/EDS-HT is to raise awareness among clinical geneticists and specialists treating chronic pain conditions about pain and other complications of JHS/EDS-HT.</span>
Answer:
Option no. c correctly describes the relationship between tissues and organs.
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(30%) gorilla babies die within the first few months of their lives because of inherent weakness of the infant or disease.
What is inherited disease?
Genetic factors play a role in almost all health conditions and traits, but there are some conditions in which genetic alterations play a role in almost all of the causes that cause the condition.
Genes are passed from parent to child, so are DNA changes within the gene. DNA changes can also occur spontaneously, first appearing in children of unaffected parents. This is called a new mutation, and the word mutation means change.
Therefore, (30%) gorilla babies die within the first few months of their lives because of inherent weakness of the infant or disease.
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If the population/number of the things they need decrease, so will the number of the organism
Answer:
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Explanation:
Most carbohydrate digestion occurs in the small intestine, thanks to a suite of enzymes. Pancreatic amylase is secreted from the pancreas into the small intestine, and like salivary amylase, it breaks starch down to small oligosaccharides (containing 3 to 10 glucose molecules) and maltose.
