De grouchy syndrome, de grouchy syndrome is a rare diesis that takes place normally in the 18q cell. 18q is a chromosomal condition that happens when a piece of a long arm witch is described as - (q) is missing from the 18 cell. Some symptoms that occur with de grouchy syndrome are your ears, your mouth shape, and your sexual develop meant. De grouchy can affect more things like having a higher chance of sezers and autistic behavior. IN most cases you will be born with de grouchy syndrome, otherwise you will be diagnosed early in life. You will be able to tell if the person has de grouchy syndrome bye their physical appearance and mental retardation. There is no official cure yet to be discovered, but there is a cure for instance people might
Rett syndrome is a postnatal neurodevelopmental disorder that mainly affects girls but is rarely found in boys as well. Rett syndrome strikes all racial and ethnic groups, and occurs worldwide in 1 of every 10,000 female births. It was first identified by Dr. Andreas Rett, an Austrian physician who described it in an article published in 1966. Even though Rett described the disorder in his 1966 article it went another 17 years until being generally recognized after Swedish researcher Dr. Bengt Hagberg published an article about the disorder in 1983 (Rett Syndrome Fact Sheet).
Nonspeech signs associated with hypokinetic dysarthria may include characteristics dealing with the face, eyes, hands, arms, and trunk. The individual may have an expressionless look to their face as well as weakness with gestures in the hands, arms, and face that would normally match the person’s prosody when speaking. Overall, their social interaction with others can be emotionless. Eye blinking occurs less frequently than normal and their head gaze does not match where their eyes are looking. These patients swallow infrequently which leads to drooling. A tremor may be present in the jaw, lips, and tongue as well as limited movement during speech even though strength of these structures is often normal.
Pierre Maroteaux was the first person to mention dwarfism. He is largely credited for the discovery. He discovered the link between the genetic condition and prenatal micromelic in patients. The discovery was known as Lamy-Maroteaux Syndrome which is a very important topic when you are talking about dwarfism. In 1994, Pierre and his team discovered the reasoning behind dwarfism. (who discovered it? March 28, 2014.) The prognosis for achondroplasia has a normal life expectancy. There are just some health issues that come with this genetic disorder like a large head, crowded teeth, bowed legs, shortened trunk, and weak hands. They are still able to do everyday things, they just have to have to be able to conform to the everyday life. Some people think that dwarfs are not as intelligent as a normal sized person but they are. Some dwarfs even go into medical school and become doctors just like an average person would. (right diagnosis March 28, 2014.)
Muscular Dystrophy is a genetic disorder in which your muscles drastically weaken over time. Muscles are replaced with “connective tissue,” which is more of a fatty tissue than a muscular one. The connective tissue is the tissue that is commonly found in scars, and that same tissue is incapable of movement. Although Muscular Dystrophy affects muscles in general, other types affect certain groups of muscles, and happen at different periods throughout a lifetime. For example one of the most common types, Duchenne Muscular Dystrophy, targets muscles in the upper thigh and pelvis. The disease is displayed throughout early childhood, usually between ages four and seven. This genetic disorder occurs only in boys. People have difficulty sitting up or standing and lose their ability to walk in their early teens. Sadly most people die by the age of twenty. A second common type, Becker’s Muscular Dystrophy affects the same muscles as Duchenne, but first appears in teenage years. Most people with Becker’s only live into their forties (Fallon 1824-1825).
lip, skin folds at the corners of the eyes, indistinct groove on the upper lip, and an
Human body is such an enigma. It is very fragile and there is not even a single person who did not fell sick in his lifetime. Some people suffer from minor flus and some have to undergo life-threatening surgeries. There are some who will have to take medicines all throughout their life and some face horrible treatments. But the most saddening thing is suffering from a disease that is so rare that only handful people know about it. It is such a bad luck that you are one in a million who is suffering from a weird disease.
 Mild, chronic depression has probably existed as long as the human condition, although it has been referred to by various different names. The DSM-III replaced the term “neurotic depression” with dysthymic disorder--which literally means ‘ill-humored’-and it was added to the Diagnostic and Statistical Manual of Mental Disorders, 1980
affect several age groups. Children can develop GAD and suffer from it the rest of their lives.
According to Hassold and Sherman (2002), the probability of giving birth to a child with DS is not linked to any race, ethnicity, socioeconomic status or geographic location. Maternal age seems to be the only etiological factor that may cause DS. Some characteristics of DS include: deep folds at the corners of the eyes, hypotonia, short stature, flexible joints, small oral cavity and heart defects (Taylor, Richards, & Brady, 2005). Most individuals with DS have a moderate intellectual disability, although there is a range of disability, from severe to high functioning (IQ above 70). Since DS is a birth defect and not a disease, there are no treatment options.
Ben’s case, there is no cure and probably never will be. He was born with this disorder and he
Autism is not a disease, but a developmental disorder of brain function. People with classical autism show three types of symptoms: impaired social interaction, problems with verbal and nonverbal communication and imagination, and unusual or severely limited activities and interests. Symptoms of autism usually appear during the first three years of childhood and continue throughout life. Although there is no cure, appropriate management may foster relatively normal development and reduce undesirable behaviors.
...appen to anyone. The person can experience feelings of hopelessness, worthlessness, unacceptance, withdrawal, and thoughts of suicide. There is no exact cause and there is no prescribed cure. Depression seems to be caused by life situations and if the symptoms of depression seem to last more than two weeks then it is classified as Major Depressive Disorder. Symptoms of SAD will resemble Major Depressive Disorder. There are many treatments for Major Depression Disorder but how good the treatment works depends on the person.
As a student who is interested in psychology and the way the brain works/functions, learning about the somatic symptom disorder intrigues me. I have never actually heard of this disorder before, but hypochondria is about the closest to a somatic disorder that I have learned about. Now, the first thing that really caught my attention about this disorder was the definition about it, “People with somatic symptom disorder become excessively distressed, concerned, and anxious about bodily symptoms that they are experiencing, and their lives are greatly disrupted by the symptoms” (Comer, 2014). This blew my mind. I had always know about people thinking they have had every sickness or believe they are suffering from something they are not, I am also aware of the placebo effect, but the fact that people can create such strong distress in their lives from bodily symptoms they experience is something that brought out my curious nature of why and how. Another thing that is very interesting to me is that there are two patterns of somatic symptom disorder, called somatization pattern (the individual experiences a large and even varied number of bodily symptoms) and predominant pain pattern (which is the individual’s primary bodily problem being the experience of pain) (Comer, 2014).
According to the DSM-5 (American Psychiatric Association, 2013), typical sadness due to experiences differs from Chris’s sadness due to the severity of symptoms and the duration causing significant impairment. Chris reported a change in daily functioning for more than two weeks with depressed mood and loss of interest in activities. The differential diagnosis for sadness is ruled out because Chris presented with symptoms in the past two weeks that consist of changes and impairment in his daily functioning as well as suicidal ideation with a plan and the intention to act. Client states that he experiences “worthless and guilt over losing both, his job and girlfriend.” According to the DSM-5 (American Psychiatric Association, 2013), the client does not meet this diagnosis for sadness.
...omosomes or genetic/chromosomal disorders. The most common type of genetic or chromosomal disorder is Down Syndrome or trisomy 21 (Cherry, n.d.). The condition occurs when a child has three chromosomes at the site of the twenty-first chromosome rather than the normal two. Some of the most common signs of Down Syndrome include round face, thick tongue, slanted eyes, hearing problems, heart defects, and intellectual impairment.