Genetics

NameProfessorSubjectDateAngelman SyndromeIntroductionAngelman syndrome , a neuro agenttic disease , was first delineated by Dr hassle Angelman in 1965 through intensive examination on the wear out on children . The inactivation of a component for ubiquitin-protein ligase orUBE3A which is similarly fit(p) in chromosome 15 causes mutation resulting to Angelman syndrome (Niemitz and Feinberg 599 . This mutation triggers delayed perplex skills victimization , seizures , jerky-puppet stance , cognitive skills impairments , paroxysmal laughter , wording defects , stick out tongue and prognathism . In the course of harvest and development , the UBE3A gene is transmitted by the father into the publication while the maternal allele shapes the brain (Niemitz and Feinberg 599 . Meanwhile , the sideboard of the pioneer researches c onducted by Dr . Angelman on the mysterious happy-puppet syndrome has led to the designation of chromosomal aberrations on 15q11-13 as the prime cause of the disease (Pelc , Cheron and Dan 578 .

As progresses , the factors that speed 15q11-13 chromosomal aberrations were successfully traced that led to the feature of the Angelman syndrome from Pader-Willi syndrome . Specifically , the typeface of the UBE3A gene in the brain was named as the major perpetrator for the occurrence of the disease . Physiologically , lone(prenominal) maternal allele is typically expressed in definite regions of the brain . The absen ce seizure of UBE3A gene leads to the 15q11-! 13 deletion from maternally inherited chromosome , paternal UPD , UBE3A gene mutation , and imprinting pertain mutation (Pelc , Cheron and Dan 578 . Since UBE3A gene was identify the phenotypic may bring back cues on the underpinning genetic instrument of the disease . This...If you want to get a full essay, come in it on our website: OrderCustomPaper.com

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