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Dwarfism News
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Primordial
Dwarfism Remains Focus of Media in New Documentary
primordialdwarfism.com -
Sep. 10, 2009
The
subject of Primordial Dwarfism has been featured in many
documentaries in recent years, made by such respected
organizations as the BBC, National Geographic, and Discovery
Network. The most recent entry in the documentary history of
Primordial Dwarfism is "Growing Up Tiny - Kenadie's
Story", which features 6-year old Kendaie Jourdin-Bromley
and her family. Footage taken at the Little People of America
cannual convention in Brooklyn, NY was featured in the
documentary. The film aired on TLC earlier this week, and will
undoubtedly be replayed several times in future months. More
information about Kenadie can be found on her website at: http://littlekenadie.com/
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Guinness
Book of Records Recognizes He Pingping as World's Shortest Man
primordialdwarfism.com -
Sep. 25,
2008
A 20-year-old man, who is just 29 inches tall and weighs just 16lb, has entered the Guinness World Records book for being the worlds shortest man.
He Pingping is the same height as an average one-year-old child, but weight wise a one-year-old child weighs more than him.
Pingping is from Inner Mongolia, and upon being discovered he was taken on a tour to the UK.
Soon after being recognized in the 2008 Guinness Book, He
began touring the world to promote the release of the Book,
and was photographed alongside several of the tallest people
in the world, including 7' 9" Bao Xishun, currently
recognized as the tallest man alive. You can learn more about
He Pingping on Wikipedia, or by visiting his Facebook page at:
http://www.facebook.com/therealpingping
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Aditya
'Romeo' Dev Requires Surgery for Life Threatening Aneurysms
primordialdwarfism.com -
Sep. 21,
2008
Aditya
'Romeo' Dev, who was cited in the Guinness Book of records as
the World's Smallest Bodybuilder received some frightening
news after a recent MRI. He has several serious brain
aneursyms, which left untreated, will soon burst, causing
massive stroke and death. Aditya needs surgery to correct
these aneurysms as soon as possible. Doctors at Narayana Hrudayalaya Hospital
in Bangalore have agreed to do the surgery for a greatly
reduced rate, but Aditya's family is having trouble raising
the money they need to help save his life. A website has been
set up at http://www.romeodevofficialwebsite.com
to help raise money for Aditya's surgery. Please take a minute
to visit the site and if at all possible help Aditya and his
family in their hour of need.
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Participation
in study of Primordial Dwarfism sponsored by Potentials
Foundation
potentialsfoundation.org -
Apr. 4,
2008
The Potentials Foundation is sponsoring a registry of individuals with Microcephalic Osteodysplastic
Primordial Dwarfism Type II
(MOPD II) and other related forms of primordial dwarfism. The purpose of
this registry is learn more about MOPD II and how to predict and treat medical problems and conditions
that arise as a result. The name of the registry is “The Potentials Foundation Primordial Registry at
A.I. duPont Hospital for Children”. Dr. Michael Bober at Alfred I. duPont Hospital for Children is the
physician in charge of this registry. The following other specialists are also involved: William Mackenzie,
MD, Orthopedics, A.I.
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Scientists
question whether fossil remains found on Isle of Flores are
early examples of Primordial Dwarfism
anthropology.net - Jan. 8,
2008
Following
Dr. Anita Rauch's discovery of the genetic mutation that
causes MOPD II, speculation has begun as to whether the fossil
remains found last year on the Isle of Flores might not
actually represent a new species of hominid, but simply be
early examples of homo sapiens affected by Primordial
Dwarfism.
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Mutations
in the Pericentrin (PCNT) Gene Cause Primordial
Dwarfism (MOPD II)
sciencemag.org - Oct. 1,
2007
A
study conducted by Dr. Anita Rauch in Germany has determined
that MOPD II is caused by a mutation in the Pericentrin (PCNT)
gene on chromosome 21. The link above points to a short
abstract of the article by Dr. Rauch, and offers a link to
purchase the full article. Families of affected MOPD II
children can contact the administrator of this site for more
details about the information contained in the article.
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