Hutchinson-Gilford Progeria Syndrome

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Hutchinson-Gilford Progeria Syndrome This paper is on the Hutchinson-Gilford Progeria Syndrome. The paper will first define Hutchinon-Gilford Progeria Syndrome. This paper will discuss the signs and symptoms of Hutchinson-Gilford syndrome. Finally this paper reviews the prognosis of Hutchinson-Gilford Progeria syndrome. This paper is on the Hutchinson-Gilford Progeria Syndrome (Englert .C. 2009). Hutchinson- Gilford Progeria Syndrome is a genetic condition characterized by appearance of advance aging in children (Englert .C. 2009). Ninety percent of children with Progeria have a mutation set of genes (Englert .C. 2009). The gene is passed from a family member, sometimes it occurs without cause (Englert .C. 2009). It is very rarely seen in more than one child in a family. Progeria is Greek and means “prematurely old’ (Englert .C. 2009).There are different forms of Progeria, the classic type is Hutchinson- Gilford Progeria Syndrome (Englert .C. 2009). Progeria was named after the doctors who first discovered it in England (Englert .C. 2009). In 1886 it was Dr. Jonathan Hutchinson, and in 1897 it was discovered by Dr. Hastings Gilford (Englert .C. 2009). There are many signs and symptoms of Hutchinson-Gilford Progeria Syndrome (Englert .C. 2009). Some are slowed growth with below-average height and weight, hair loss, including eyelashes and eyebrows (Englert .C. 2009). Patients are born looking healthy; children with Progeria begin to display the characteristics from 18-24 months (Englert .C. 2009). The prognosis of Hutchinson-Gilford Progeria Syndrome is associated with a short lifespan (Englert .C. 2009). The lifespan is usually 18-21years some patients can live up to thirty years (Englert .C. 2009). The cause of death is related to the heart or a stroke (Englert .C. 2009). There are no treatment or cures for Hutchinson - Gilford Syndrome (Englert .C. 2009).

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