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    Aarskog Syndrome Description Aarskog syndrome (also known as Aarskog–Scott syndrome‚ faciodigitogenital syndrome‚ shawl scrotum syndrome and faciogenital dysplasia) is a rare autosomal X-linked inherited disorder that affects a person’s height‚ muscles‚ skeleton‚ genitals‚ and appearance of the face. It mostly affects at birth and the symptoms usually become apparent by the age of 3years. Unfortunately‚ Aarskog syndrome is a lifelong condition without a cure. Some people with Aarskog syndrome are born

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    Prognosis The prognosis for Williams Syndrome is not bright in some areas and bright in others. Since there is no cure for this genetic disorder‚ treatment in no way can change the prognosis unless it is to alleviate a symptom of this disorder. Cardiovascular symptoms aside‚ individuals suffering from this disorder can live a healthy and long life if properly cared for and nurtured‚ but this is very rare. There are several ways to discuss the prognosis for this disorder and they are: life expectancy

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    Countless people around the world suffer from Carpal Tunnel Syndrome. Or in other words‚ a numbness and tingling in the hand and arm caused by a pinched nerve in the wrist. Many citizens believe that the issue of Carpal Tunnel Syndrom may be a personal problem. Although‚ in reality it is a major political issue. Many workers miss days at a time because of the pain that working brings. “The median nerve runs from your forearm through a passageway in your wrist (carpal tunnel) to your hand. It provides

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    Townes-Brocks syndrome is an autosomal dominant inheritance syndrome that is caused by mutations in SALL1‚ which is located on 16q12.1 and whose gene product is a zinc finger protein that acts as a transcription factor gene (Kohlhase 2016). This syndrome is often caused by a variety of mutations such as nonsense‚ frame-shift‚ deletions‚ duplications and insertions. More severe cases have been related to a dominant negative or positive effect of a truncated protein (Stevens and May 2016). The prevalence

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    Sotos Syndrome‚ Pediatric Sotos syndrome is a disorder that results in increased growth during childhood‚ clumsiness‚ and delay in mental development. Over time‚ many children with Sotos syndrome catch up in mental development. Physical growth eventually slows down. By puberty‚ most children with Sotos syndrome are similar in size to other children their age. Most children with this disorder grow up and lead normal lives. CAUSES The cause of Sotos syndrome is a mutation in a gene. The gene

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    Introduction: Hurler Syndrome (MPS-I)‚ otherwise classified as Mucopolysaccharidosis‚ is the most severe form of this disease and is caused by cells being unable to break down dermatan sulfate and heparan sulfate during regular metabolism(Laberge‚ 2010). The build up of these two by-products disturbs regular cell functionality and this may cause damage within the tissues of organs (Laberge‚ 2010). Two major symptoms found within an individual with Hurler Syndrome are skeletal deformities and

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    the inside. The article called “Indoor Pollution and Sick Building Syndrome Symptoms”‚ by Chi-Shan

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    urinate a lot‚ always thirsty‚ and stress‚ oh no these signs and symptoms are Cushing syndrome and diabetes insipidus‚ which are Pituitary gland diseases. Then I start reading and found out that‚ Pituitary gland is a tiny organ the size of a pea found at the base of the brain behind your nose and between your ears. Pituitary gland produces a number of hormones or chemicals

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    interesting (amusing‚ entertaining‚ worth reading‚ boring‚ dull). Why? 7. Character sketches. 8. An episode you like most. The title of the book I’ve read is one flew over the cuckoo’s nest. Cuckoo’s nest according to American interpretation is a mental hospital‚ and “one flew over the cuckoo’s nest” means that one could escape from the Combinate to freedom. This novel was written by an American writer Ken Kesey in 1959 and became one of the most popular books of the 20th century. The book

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    Robert’s Syndrome or Psuedo Thalidomide Syndrome is a gentic disorder with many growth delays before and after birth. This syndrome shows the malformation of legs and arms‚ abnormalalitles of the skull and facial regions. In most cases‚ it causes intelutcal disabitlly. In a case presneted‚ the parents of four children‚ the third conception had Robert’s Diesase. However the child was not diagnosed till the age of two. The only sign at birth was a cleft palate. At the age of two‚ the child was unable

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