Galactokinase deficiency

spend a lot of time participating in outside activities. Genetic defects also make a small impact to the numerous emphysema cases. The lack of a protective protein called alpha 1-antitrysin is a defect that can be inherited. Alpha 1-antitrypsin deficiency-related emphysema is rare but it can occur. When it comes to genetics and inheriting alpha- 1 antitrypsin emphysema cannot be controlled. However, an individual can regulate their own activities and the place where they reside. Let’s take a person

Alpha-1 Antitrypsin Deficiency Alpha-1 antitrypsin (AAT) is a protein that helps the lungs and other organs work properly. It is made by the liver. AAT deficiency is a genetic condition that happens when the liver produces too little AAT, no AAT, or AAT that does not work properly. AAT deficiency can cause liver disease, lung disease, and a skin condition called panniculitis (rare). Exposure to things like smoke and dust can make AAT deficiency worse. CAUSES AAT deficiency is caused by a genetic

COPD COPD is a term used for Chronic obstructive pulmonary disease. This is an “obstructive disease”, meaning that airflow coming out of the lungs during exhalation is blocked. The blockage of airflow with COPD ,makes it very difficult for a person to breathe. Over time, COPD get progressively worse because doctors have not yet found a cure. COPD affects more Than 5% of the adult population, and is a major cause of morbidity and mortality in the United States and worldwide. 4 With COPD

Otherwise known as G6PD deficiency, people with an extreme case of this illness would experience hemolytic anemia, fever, and fatigue after eating fava beans or take drugs like primaquine. This is due to the fact that people with favism lack sufficient amount of the enzyme G6PD,

While many believe that diseases and viruses are only harmful, Dr. Sharon Moalem explained how many different diseases actually helped humans survive through many hardships. Moalem writes, “Why would you take a pill that was guaranteed to kill you in forty years? Because it will save you tomorrow. Why would we select for a gene that will kill us through iron loading by the time we reach what is now Middle Ages? Because it will protect us from a disease that is killing everyone long before that.”

The first disease that will be discussed is hemochromatosis. Hemochromatosis mainly targets the liver, heart, pancreas, joints, testicles, thyroid, and skin organs. The symptoms of hemochromatosis include: “liver failure, heart failure, diabetes, arthritis, infertility, psychiatric disorders, and cancer.” Hemochromatosis was first described by Armand Trousseau in 1865. Then, in 1889 Friedrich Daniel von Recklinghausen coined the term hemochromatosis. Afterwards, a group of California scientists isolated

Moalem allows us to grasp the knowledge that our cells are not the only ones that benefited our longevity of life, but the stuff that can kill us, has also done the trick. Hemochromatosis, Diabetes, and Glucose-6-phosphate-dehydrogenase deficiency (G6PD deficiency or favism), are all things that can kill is easily without the proper treatment. However, long ago, these are the same that would help us live longer. Basically evolution wanted you to live another 5 years, then another 5 days. Hemochromatosis

For this writing assignment, you will select one article from the Suggested readings posted on Blackboard, and type a response for each of the questions listed below. Please find additional guidelines in the file “Writing assignment guidelines” posted on Blackboard. Please provide the following information: Title: _______Fetal Testosterone Predicts Sexually Differentiated Behavior in Girls and in Boys____________________________________________________________________ Author/s: ____Bonnie Auyeung