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(Hutchinson-Gilford Progeria Syndrome)




    By Alexis Goll & Ahliyah Reed
Progeria, or Hutchinson-Gilford Progeria Syndrome (HGPS),
is a genetic disorder caused by a gene-mutation that
results in rapid aging in humans. It is extremely rare, and
often just “pops up” in a family. It is believed to be a non-
hereditary disorder, but it is possible that this disorder has
the potential to be hereditary.



There are about 130 cases of this disease
reported ever, about 1 in 4 million babies
have been born with it worldwide. Most
Of these kids don’t live past 13.
   The word “Progeria” means “prematurley-old” in Greek.
   Named after the scientists who discovered it, Dr. Jacob
    Hutchinson in 1886 and Dr. Hasting Gilford in 1904.
   Major reasearchers of Progeria:
        -Dr. Francis Collins, who discovered the gene.
        -Doctors at the National Human Genome Research
        Institute (NHGRI).
        -Dr. Hutchinson & Dr. Gilford.



                        Dr. Francis Collins, who played
                        an extremely important role in
                         not only the discovery of the
                            LMNA gene, but the entire
                             Human Genome Progect.
Because of the obscurity of the illness, an exact
reason why this happens is still unknown-of.
But, the cause of Progeria occurs because of a
mutation in a gene called LMNA.
LMNA is a gene that produces the protein Lamin-A,
which gives the cells’ nucleuses’ structural support.
Because of the unstable nucleuses in the bodys’ cells,
Progeria occurs.



                               Unstable,
                          mutated forms
                           of the LMNA
                                  gene.
There are some early signs of Progeria
that are visibly noticeable:
 Shortened period of growth, stops at
  around 6 months to a year.
 Hair loss or lack of hair


      Scientists can confirm if a
        child has Progeria from
          genetic testings for a
         mutated LMNA gene.
   Stunted growth, small stature

   Loss of all hair, including eyelashes and eyebrows

   Weak, fragile bones and teeth

   Narrowed face and pointed nose

   Heart conditions and failure (these usually are the cause of death)

   Head un-proportionally large in comparison to body

   Little muscle tone and stiff joints (causes motor-skill problems)

   Visible veins on skin, hardened skin

   High-pitched voice

   Lowered jaw, prominent eyes, and thin lips
Children with Progeria do not live long because of the state their bodies
are in before they hit puberty; they have the bodies of 80 year old
people. Victims will die usually due to heart failure/disease brought on
by the disorder.

                                The average life-span of someone with
                                Progeria is13 years. However, deaths
                                have ranged from 9 months to about 22
                                years.



                                 Diagram of Atherosclerosis, or
                                 hardening of the arteries, which is the
                                 main cause of death for people with
                                 Progeria.
There is no cure for Progeria, but there are
some things the families of those who have it
can do to make their lives less miserable.

  Regularly take asprin
 Small meals
 Weekly checkups
 Physical therapy and mild physical activity
 Removal of primary teeth
 Other medications for pain.
http://www.progeriaresearch.org

     http://www.mayoclinic.com

   http://www.health.nytimes.com

     http://www.ghr.nlm.nih.gov

http://www.hayleyspage.com/progeria

 http://www.rareglobaldiseases.com
Everything you Need to Know About Progeria

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Everything you Need to Know About Progeria

  • 1. (Hutchinson-Gilford Progeria Syndrome) By Alexis Goll & Ahliyah Reed
  • 2. Progeria, or Hutchinson-Gilford Progeria Syndrome (HGPS), is a genetic disorder caused by a gene-mutation that results in rapid aging in humans. It is extremely rare, and often just “pops up” in a family. It is believed to be a non- hereditary disorder, but it is possible that this disorder has the potential to be hereditary. There are about 130 cases of this disease reported ever, about 1 in 4 million babies have been born with it worldwide. Most Of these kids don’t live past 13.
  • 3. The word “Progeria” means “prematurley-old” in Greek.  Named after the scientists who discovered it, Dr. Jacob Hutchinson in 1886 and Dr. Hasting Gilford in 1904.  Major reasearchers of Progeria: -Dr. Francis Collins, who discovered the gene. -Doctors at the National Human Genome Research Institute (NHGRI). -Dr. Hutchinson & Dr. Gilford. Dr. Francis Collins, who played an extremely important role in not only the discovery of the LMNA gene, but the entire Human Genome Progect.
  • 4. Because of the obscurity of the illness, an exact reason why this happens is still unknown-of. But, the cause of Progeria occurs because of a mutation in a gene called LMNA. LMNA is a gene that produces the protein Lamin-A, which gives the cells’ nucleuses’ structural support. Because of the unstable nucleuses in the bodys’ cells, Progeria occurs. Unstable, mutated forms of the LMNA gene.
  • 5. There are some early signs of Progeria that are visibly noticeable:  Shortened period of growth, stops at around 6 months to a year.  Hair loss or lack of hair Scientists can confirm if a child has Progeria from genetic testings for a mutated LMNA gene.
  • 6. Stunted growth, small stature  Loss of all hair, including eyelashes and eyebrows  Weak, fragile bones and teeth  Narrowed face and pointed nose  Heart conditions and failure (these usually are the cause of death)  Head un-proportionally large in comparison to body  Little muscle tone and stiff joints (causes motor-skill problems)  Visible veins on skin, hardened skin  High-pitched voice  Lowered jaw, prominent eyes, and thin lips
  • 7. Children with Progeria do not live long because of the state their bodies are in before they hit puberty; they have the bodies of 80 year old people. Victims will die usually due to heart failure/disease brought on by the disorder. The average life-span of someone with Progeria is13 years. However, deaths have ranged from 9 months to about 22 years. Diagram of Atherosclerosis, or hardening of the arteries, which is the main cause of death for people with Progeria.
  • 8. There is no cure for Progeria, but there are some things the families of those who have it can do to make their lives less miserable.  Regularly take asprin  Small meals  Weekly checkups  Physical therapy and mild physical activity  Removal of primary teeth  Other medications for pain.
  • 9. http://www.progeriaresearch.org http://www.mayoclinic.com http://www.health.nytimes.com http://www.ghr.nlm.nih.gov http://www.hayleyspage.com/progeria http://www.rareglobaldiseases.com