By: Noel Corral and Jackie Salazar ALBINISM. GENETIC DISORDER Albinism is a recessive genetic...
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Transcript of By: Noel Corral and Jackie Salazar ALBINISM. GENETIC DISORDER Albinism is a recessive genetic...
![Page 1: By: Noel Corral and Jackie Salazar ALBINISM. GENETIC DISORDER Albinism is a recessive genetic disorder due to a defective X-chromosome In order to have.](https://reader036.fdocuments.in/reader036/viewer/2022083004/56649d9e5503460f94a87ebc/html5/thumbnails/1.jpg)
By: Noel Corral and Jackie Salazar
ALBINISM
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GENETIC DISORDER• Albinism is a recessive genetic disorder due to
a defective X-chromosome
• In order to have Albinism both parents must have a defective gene.– Statistics show that about 1 in 17,000 people suffer
from some form of albinism
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SYMPTOMS • A person with Albinism will have one of the
following symptoms:– Absence of color in the hair, skin, or iris of the eye– Lighter than normal skin and hair– Patchy, missing skin color
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DIAGNOSIS • For Diagnosis there are several ways to know
whether or not you have Albinism – Physical examination– Description of changes in pigmentation– Thorough examination of the eyes– Comparison of your child's pigmentation to that of
other family members
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PROGNOSIS• Albinism does not usually affect lifespan
• People with Albinism may be limited in their activities because they can't tolerate the sun.
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TREATMENT • There is no type of cure for Albinism for it
happens in the genetics
• There are certain recommendations for the symptoms – For the eyes: Visual aids (glasses) – For the skin: Precaution in the sunlight (use of
sunscreen)
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CURRENT RESEARCH • The National Eye Institute has come up with a
hypothesis; it being that nitisinone would improve the vision in Albinism patients.
• They are currently testing on mice with Albinism and have been able to conclude that nitisinone increases hair and eye pigmentation
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GENETIC COUNSELING • If the parents would want to know whether or not
their child had a possibility in having Albinism they would get told the following – If both parents were not albino but carried the genetic
disorder, there is a 1 out of 4 chance their baby will be born with Albinism.
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STORY ON VEDASTUS ZANGULE• Vedastus Zangule was a 13 year old albino child when
Harry Freeland went to Tanzania to make a documentary on the suffering albino kids.
• Harry met Vedastus and filmed him and several other albino kids because they were getting bullied at school and threatened by their community
• After the video was published an organization for the funding of his education was started and financial aid for his family was given.
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CREDITS • "Albinism - Types - Symptoms - Diagnosis - Treatment - FAQs | Medindia." Medindia -
Medical/Health Website. Web. <http://www.medindia.net/patients/patientinfo/albinism.htm>.
• "What Happened To Vedastus Zangule After The Documentary?!." Southern Africa's Children UK Charity. Web. <http://www.southern-africas-children.org.uk/what-happened-to-vedastus-zangule.html>.
• " Is Albinism Treatment On The Anvil? | Medindia." Medindia - Medical/Health Website. Web. <http://www.medindia.net/news/Is-Albinism-Treatment-On-The-Anvil-91238-1.htm>.
• "What Is Albinism? What Causes Albinism." Medical News Today: Health News. Web. <http://www.medicalnewstoday.com/articles/245861.php>.
• "Albino Stories." Southern Africa's Children UK Charity. Web. <http://www.southern-africas-children.org.uk/albino-stories.html>.
• "Albinism: Tests and diagnosis - MayoClinic.com." Mayo Clinic. Web. <http://www.mayoclinic.com/health/albinism/DS00941/DSECTION=tests-and-diagnosis>.
• "Albinism - PubMed Health." National Center for Biotechnology Information. Web. <http://www.ncbi.nlm.nih.gov/pubmedhealth/PMH0002450/>.