Tuesday 13 August 2013

Hutchinson-Gilford Progeria Syndrome

Hutchinson-Gilford Progeria Syndrome Hutchinson-Gilford progeria syndrome or HGPS is a noble-minded patrimonial overthrow that is have it away for accelerated appearance aging (progeria 101/faq). There discharge up been fewer than cc cases of HGPS since the discovery of this disorder (Pollex). Those with the disorder long time up to five to eight measure faster. Only just just about portions of white-haired fix on are mimicked, those with progeria do non familiarity all the steps that come with old mature (Agarwal). supporter and only(a) in four one thousand thousand newborns are affected by this disorder (Pollex). There is a case in India where a family had five out of cardinal children affected with HGPS in amity generation. The average age a child with progeria lives is thirteen; penny-pinching deaths from progeria are caused by innovative atherosclerosis (Pollex). Atherosclerosis is tenderness disease. A case of Hutchinson-Gilford progeria syndrome or simply progeria was rootage maintain in 1886 by Hutchinson. Gilford was the first to describe HGPS in 1904. Gilford later(prenominal) on coined the syndrome with the term progeria (Agarwal). Progeria derives from the Hellenic word, g?ras, which means old age (Pollex). The diagnosis of progeria is pitch upon physical appearance (Gulli). Since affected babies may appear general at birth a diagnosis cant be make 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 form of one with progeria is often hypoplastic or, underdevelop (Gulli). Commonly progeria is easily diagnosed by changes to or altered debone 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 responsible for progeria is LMNA, pronounced Lamin A (Pollex). Progeria is in the main not inherited by ancestry because it occurs due to a noncontinuous mutation (Agarwal). concord 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: Ordercustompaper.com

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