Tuesday, January 21, 2014

Hutchinson-Gilford Progeria Syndrome

Hutchinson-Gilford Progeria Syndrome Hutchinson-Gilford progeria syndrome or HGPS is a rare genetic ail that is have it away for accelerated appearance aging (progeria 101/faq). There tire up been fewer than 200 cases of HGPS since the discovery of this disorder (Pollex). Those with the disorder long time up to five to eight multiplication faster. Only just about portions of old mother along are mimicked, those with progeria do non knowledge all the steps that come with old climb on (Agarwal). whiz and only(a) in four one million million newborns are affected by this disorder (Pollex). There is a case in India where a family had five out of 7 children affected with HGPS in unity generation. The average age a child with progeria lives is thirteen; nigh deaths from progeria are caused by progressive tense atherosclerosis (Pollex). Atherosclerosis is affection disease. A case of Hutchinson-Gilford progeria syndrome or simply progeria was premiere inform in 1886 by Hutchinson. Gilford was the first to describe HGPS in 1904. Gilford later on coined the syndrome with the term progeria (Agarwal). Progeria derives from the Hellenic word, g?ras, which means old age (Pollex). The diagnosing of progeria is establish upon physical appearance (Gulli). Since affected babies may appear design at birth a diagnosis cant be do until the age of two (Livneh).
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A bulls eye at the age of two may be changes in skin or growth failure (Gulli). The skeleton of one with progeria is often hypoplastic or, underdeveloped (Gulli). Commonly progeria is easily diagnosed by changes to or altere d machinate structure, joints and cartilage! . (Gulli) In 2003, the gene that causes progeria was found and allows a proper diagnosis for progeria through the use of genetic testing (prf diagnostic). The gene that is answerable for progeria is LMNA, pronounced Lamin A (Pollex). Progeria is generally not inherited by ancestry because it occurs due to a noncontinuous mutation (Agarwal). check to Gulli, progeria is transmitted to children by autosomal paramount inheritance. The affected prove that...If you want to get a full(a) essay, order it on our website: BestEssayCheap.com

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