Syndrome Essay

Hans Asperger, a pediatrician from Austria, began to study a group of children at his clinic in 1944. He noticed that the young boys he was studying were clumsy, lacked social skills, and did not understand nonverbal communication. Asperger’s syndrome (AS), named after Doctor Hans Asperger, is a developmental disorder. Research by Woodbury-Smith and Volkmar (2009), claim that AS was originally thought of as a less severe form of Autism, in which the individual has higher linguistic ability but still

motor tics or vocal tics that have been present for more than a year, and individuals with Provisional Tic Disorder have tics that have been present for less than a year. Medications could used to reduce motor tics or vocal tics caused by Tourette syndrome. For example pimozide is a medication that works by decreasing the activity of dopamine in the brain. In many instances, no treatment is needed, tics could resolve automatically; in other cases behavioral therapy with the suggestion of “life style

Asperger’s syndrome is becoming more and more common as time goes by. Each year, more children are being diagnosed. This paper focuses on Asperger’s Syndrome and developing social skills in various social settings. By looking at the etiology, diagnostic procedures, how the condition effects development, daily challenges, current social/cultural views, and relevant social interventions, a better understanding on how to develop social skills for children with Asperger’s Syndrome can ensue. The

Duane retraction syndrome (2013 ICD Code 378.71), or Stilling–Turk–Duane syndrome, is now a commonly recognized abnormality of ocular motility. The condition is considered as congenital cranial dysinnervation disorders. The incidence is approximately 0.1% part of the general population. 1% to 5% of strabismus patients are likely to have DRS of which 15% are bilateral (1)(2)(3)(4)(5). It is more common in girls (60%) than boys (40%) and left eye is three times more likely to be involved than right

FRAGILE X SYNDROME Fragile X Syndrome (FXS) also known as , the Martin-Bell, or the marker x syndrome. This genetic disorder is an autosomal dominant. It is a genetic condition that causes a range of developmental problems including learning disabilities and cognitive impairment. Majority of the time males are in more risk than females to getting this genetic disorder. For more proof of this fact statistics say that 1 in 4,000 males and 1 in 8,000 females tend get this disorder.This disorder

Sjogren’s syndrome (SS) is a chronic, systemic autoimmune disease characterized by keratoconjunctivitis and xerostomia results from infiltration of the lacrimal glands and salivary glands by lymphocytes. It occurs worldwide and in all age groups with a female predisposition. It may exist as primary or secondary SS. Oral manifestations of SS may help in early diagnosis and management of the disease. We present a case report a comprehensive literature review of sjogren’s syndrome. KEYWORDS: Sjogren’s

journal articles, texts, and websites. Though, texts and web information were both used in a limited capacity. The literature review specifically focuses on the effect the syndrome has on the speech and language of affected individuals. I. Characteristics Treacher Collins syndrome is also known as Franceschetti-Klein syndrome and mandibulofacial dysostosis. It was originally written about by George Andreas Berry in 1889 and next by Dr. Edward Treacher Collins in a 1990 case report. In each circumstance

A) Wolf-Hirschorn syndrome, also called deletion 4p syndrome amongst others This is a genetic disorder caused by a missing piece of chromosome 4. It is a rare disease and only affects about 1:50,000 births. The result of this missing piece on the short arm of chromosome 4 is a wide range of physical and developmental symptoms and impairments. These include microcephaly, slow growth in utero and postpartum, hypotonia, seizures, profound intellectual disability, cryptorchidism, and hypospadias, amongst

Patau Syndrome, otherwise known as T13 is a very rare and lethal genetic disorder in which a person has three copies of chromosome 13 instead of two. T13 is characterized by the presence of an assortment of heart and brain malformation in newborns. Children with the disease are often born with multiple birth defects that are normally associated with T13 but not limited to it, including small eyes, undescended testicles, cleft lip/palate, and they consistently exhibit signs of mental deficiency and/or

NEW DEVELOPMENT ABOUT ASPERGERS SYNDROME Although the current knowledge regarding the nature of Asperger syndrome and its interventions are still limited. There is an upsurge of research on the disorder that in prompted many to write books and do deeper research. Projects are underway to better improve assessment and diagnosis the condition of Asperser syndrome. As stated in so many articles awareness of Asperger syndrome is growing and so is the general interest regarding availability of service