Vitiligo is a skin condition characterized by loss of pigmentation in blotches. The cause of vitiligo is the death of melanocytes, the cells that are responsible for producing melanin. According to the National Institutes of Health and the National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS, 2014), the cause of vitiligo remains unknown. There is some speculation that vitiligo is an autoimmune system disorder, but the condition may also be caused by genetics (NIAMS, 2014). According to the American Academy of Dermatology (2017), the vitiligo is correlated with autoimmune diseases, and a person is at a higher risk for vitiligo if a family member also has the condition. Exposure to the sun may also be an issue, as the skin areas affected by vitiligo tend to be those that are most exposed such as hands and face. The primary signs of the disease are visible. The most noticeable symptom is loss of skin pigmentation on different parts of the body. There are many different manifestations of vitiligo, which can even affect hair pigmentation, the inside of the mouth, or even the iris of the eye (American Academy of Dermatology, 2017). The symptoms are primarily cosmetic, with no known related issues....
For example, there is no pain associated with vitiligo. However, vitiligo is highly visible especially in people with dark skin, and can cause psychological and social symptoms. Therefore, people who have vitiligo might develop social anxiety or low self-esteem and the condition can therefore be considered "life altering," (American Academy of Dermatology, 2017).
Psychosocial Process Recording Theories thrive in situations where facts are scarce or sparse in human endeavors. Medicine is a field in which such truths are evident. According to Gorman (1990), radical biologists hold the view that all psychiatric complications are caused by brain abnormalities. On the other hand, dogmatic psychologists claim that medical treatment only covers up psychiatric symptoms. They state that psychological treatment gets to the root of the problem
Decision-Making by Caregivers of Family Members with Heart Failure Describe the population for this study. The population for this study consisted of people who are family members of those with cardiovascular issues who may develop heart failure or who are currently living with heart failure. The intention was to find out how prepared family members were to deal with worst-case scenarios regarding the patient's care. How was the sample selected? What are
Biological Psychology: SchizophreniaIntroductionSchizophrenia is a mental disorder that is characterized by delusions, hallucinations, and distorted thinking. The exact cause of schizophrenia is unknown, but it is believed to be a combination of genetic and environmental factors. Schizophrenia has been described throughout history, with the first known case dating back to the mid-6th century BC. In ancient times, it was considered as being caused by a range of factors (from environmental
Caregiver Decision Making for Heart Failure Reading Research Literature #1 Type your answers to the following questions using complete sentences and correct grammar, spelling, and syntax. Click Save as and save the file with your last name and assignment, e.g.,NR439_RRL1_Smith. Submit to the Reading Research Literature #1 basket in the Dropbox by 11:59 PM MT Sunday at the end of Week 5. The guidelines and grading rubric for this assignment may be
Those who happen to be disproportionately affected by hypertension according to Elliot (2007) are African-Americans. Family history of BP also plays a prominent role in the prevalence of hypertension. In the words of Elliot (2007), "data consistently indicate that BP levels are hereditable." What this means is that studies have clearly demonstrated that an individual's risk of high blood pressure is largely dependent on whether or not there is
Family Communication There is a lot of information on dementia, and even a lot about the concerns that families may have about the treatment of their loved ones in facilities, however there is very little if not any research regarding communication between dementia patients and their families before and after placement in a long-term care facility. Clark, Bass, Looman, McCathy, & Eckert (2004), reported that while various quantitative and qualitative analyses have
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