Watership Down is a “modern classic” in which the story features real places with fictional characters that are rabbits. The rabbits are on a journey to find a new warren and create a new home when one rabbit named Fiver foresees the eventual destruction of their warren and demands they have to leave instantly. Hazel‚ the leader of the group and the brother of Fiver‚ has to navigate the tough terrain and landscape with the small group of rabbits that left with them to find a suitable warren to create
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Ehlers-Danlos Syndrome Ehlers-Danlos Syndrome (EDS) is an inherited connective tissue disorder that is classified into six distinct primary types. EDS was first described around the turn of the century by Eduard Ehlers‚ a Danish physician‚ and Henri-Alexandre Danlos‚ a French physician. Before 1997 there were ten recognized types of EDS that were labeled with Roman numerals I through X. Once doctors had more experience with patients with EDS and as technology improved to study biochemical
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Turner’s Syndrome Turner’s syndrome is a genetic condition in which a female does not have the usual pair of two X chromosomes. This medical disorder affects about 1 in every 2‚500 girls. I do not know exactly what causes Turner syndrome‚ but researchers know that it is the result of a problem with a girl ’s chromosomes either not being there at all or only part of it is still there. I think the most known effects of the condition vary widely with girls with Turner syndrome. It all depends
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CRI DU CHAT SYNDROME WHO DISCOVERED CRI DU CHAT SYNDROME? In 1963‚ JEROME LEJEUNE described a syndrome consisting of multiple congenital anomalies‚ mental retardation‚ microcephaly‚ abnormal face‚ and a mewing cry in infants with a deletion of a B group chromosome (Bp-)‚ later identified as 5p- WHAT IS CRI DU CHAT SYNDROME? Cri-du-chat syndrome is an autosomal deletion syndrome caused by a partial deletion of chromosome 5p and is characterized by a distinctive‚ high-pitched‚ catlike cry in infancy
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Angelman syndrome (AS) is an infrequent genetic condition that has a considerable impact on a person’s nervous system which causes them to have severe physical and intellectual disabilities; I will briefly define these in the commentary (Genetic Disorders‚ 2015). Harry Angelman identified the condition in three children in 1965 however in today’s research it is found in one in sixteen million people.(Angelmanuk.2015).Therefore the reason the research has been so motivational is due to it being very
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Brooks Quartararo Mrs. Ruble Period 3 23 February 2012 Tourette’s Syndrome Tourette’s Syndrome is a neurological disorder caused by repetitive‚ involuntary movements called tics. The disorder is named after Dr. Georges Gilles de la Tourette‚ a French neurologist who first discovered the disease in 1885. Tourette’s is an inherited disorder‚ and it’s believed that it is closely linked to damage of the basal ganglia or the brain. The tics are classified as simple or complex. Simple tics are sudden
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MENTAL RETARDATION Chapter 1 Historical Overview Introduction Pre-Independence–Changing Life Styles in India I dentification of persons with mental retardation and affording them care and management for their disabilities is not a new concept in India. The concept had been translated into practice over several centuries as a community participative culture. Changes in attitudes towards persons with disabilities also came to about with city life. The administrative authorities
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One doesn’t need to shed blood or offer his body to be burned just to become a hero. Touching lives and making a big difference is enough. Such are teachers. Teachers are our modern day yet unsung heroes. They are surrogate parents‚ molders of young minds‚ and the epitome of integrity. The school is our second home and within the portals of this institution are unsung heroes who spend their time‚ effort‚ and even money to make our educational journey worthwhile. Our teachers‚ like real moms and
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Aspergers Syndrome is a lifelong neurobiological disorder of social interaction and behavior (Frith 2004; Wing 1981; Gillberg and Gillberg 1989; Klin et al. 2000). The purpose of this study was to study the language performance in school-aged children with Aspergers Syndrome along with their age‚ sex‚ and IQ matched controls. Prior to the study‚ they expected children with Aspergers Syndrome to perform below average in the selected measures of language due to their difficulties in language development
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KLINEFELTER SYNDROME RESEARCH 1 Klinefelter Syndrome Research Duyen Le Ap Biology KLINEFELTER SYNDROME RESEARCH 2 Abstract Klinefelter syndrome is the most common genetic disorder that affects males. The affected male has an extra copy of X chromosome‚ which means he has 47 chromosomes (XXY). The effects of Klinefelter syndrome vary by age; the patients with Klinefelter syndrome usually have weak muscles‚ slow
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