Münchausen syndrome

but also the difficulties he has had to over-come and the courage he needed to get through them. This story gives a glimpse into the life of an Aspergergian- as he likes to call himself. Aspergers syndrome is a form of autism that affects the ability to effectively socialize and communicate. This syndrome generated a vast majority of complications all throughout his life. During his childhood, John is a social outcast. He does not know how to befriend people, and he is very blunt and rude to his peers

Tierani Richardson Reflection 15 Content: Our group was assigned velocardiofacial syndrome (VCFS). I was excited to receive a syndrome to which I had not been exposed. I was assigned etiology, history, and incidence/prevalence. I learned that VCFS originates from the Latin words “velum” which means “palate,” “cardia” which means “heart,” and “facies” which means having to do with the face. It is the most common syndrome associated with cleft palate! Additionally, VCFS is an autosomal dominant condition

Johnson-Munson syndrome is a rare syndrome identified by missing abnormal vertebrae, fingers and toes and various deformities of the heart, lungs, intestines, pancreas and intestines. Ophanet a consortium of European partners defines a condition as rare. In the US population, less than 200,000 people can possibly be affected by Johnson Munson Syndrome or second type of Johnson Munson syndrome. (Orphanet 2015) Johnson Munson syndrome will start within the DNA from the formation of the fetus at birth

Angelman Syndrome & Prader-Willi Syndrome Introduction Prader-Willi and Angelman Syndrome are two genetic disorders with vastly differing phenotypes linked by missing genetic imprints on the 15th chromosome’s q arm between regions 11 and 13 . While both orders result in mental deficits, their symptoms are otherwise segregated from the other in their entirety. The differences in the disorders are the result of differing DNA methylation patterns present in maternally and paternally inherited DNA

Disability Research Activity (Prader-Willie Syndrome) Disability Prader-Willie Syndrome a rare congenital disorder characterized by learning difficulties, growth abnormalities, and obsessive eating, caused especially by the absence of certain genes normally present on the copy of chromosome 15 inherited from the father. Characteristics & Effects • Short stature • Small hands and feet • An abnormal body composition (reduced lean tissue and increased fat mass) • Developmental delay • Mild

If a clinician is going to individualize an assessment specifically towards a client, then in order to work on the areas identified, the intervention plan must reflect the results of the assessment. Every individual varies greatly, and with Noonan Syndrome, it is no different. Even though specific characteristics are identified, each patient will present with different degrees and attributes, if they even present with any at all. Intervention needs to be specifically designed for the individual and

William Syndrome What is Williams Syndrome? The William syndrome is also known as WS, WMS and Williams-Beuren Syndrome (WBS). WS is an uncommon genetic disorder that is present at birth which can also affect females and males equally of any culture. The characteristic facial appearance and loving personality is what makes this rare syndrome to be unique. Most affected individuals with WS can have from mild to moderate retardation.According to the Williams Syndrome Association 20,000 people are affected

Toxic shock syndrome is a rare, life-threatening complication that is the outcome of certain types of bacterial infections. It is caused by the release of poisonous substances due to an overgrowth of the bacteria Streptococcus aureus, or strep, which is found in the bodies of most women. Toxic shock syndrome has historically been associated primarily with the use of superabsorbent tampons. However, due to this fact most manufacturers have pulled certain types of tampons off the market; which has

common as hypothyroidism, it still manages to affect around fifteen-million people each year. Cushing’s disease is a condition where the body is exposed to a high amount of cortisol. This syndrome can be caused in two ways. The first way this is that the body itself produces too much cortisol (“Cushing’s Syndrome,” n.d). The second way is when a person takes a corticosteroid medication (Mayo Clinic Staff, 2010). During both ways, the excessive cortisol causes the body to “shift energy in the form

Have you ever had 27 surgeries ? Have you ever HAD to take care of your younger sister? Well Auggie had 27 surgeries and edward HAD to take care of his little sister. Both Auggie and edward worked very hard to have what they have. Wonder By RJ Palacio with Auggie is a wonderful book a heart string puller and you can laugh as well . Edward’s Eyes by Patricia MacLachlan With Edward is definitely are heart string puller with laughs and tears. Edward and Auggie are also very caring and loving. Auggie