Presentation is loading. Please wait.

Presentation is loading. Please wait.

Rachel Wells. » Warren Tay, 1881 ˃Observed symptomatic red spot in retina of eye » Bernard Sachs, 1887 ˃Described cellular changes in disease ˃Noticed.

Similar presentations


Presentation on theme: "Rachel Wells. » Warren Tay, 1881 ˃Observed symptomatic red spot in retina of eye » Bernard Sachs, 1887 ˃Described cellular changes in disease ˃Noticed."— Presentation transcript:

1 Rachel Wells

2 » Warren Tay, 1881 ˃Observed symptomatic red spot in retina of eye » Bernard Sachs, 1887 ˃Described cellular changes in disease ˃Noticed high frequency of occurrence in Ashkenazi ˃Jew population

3 » Autosomal recessive disorder » Caused by defective gene on chromosome 15 » Occurs due to the lack of hexosaminidase A ˃Hex A helps break down gangliosides in nerve tissue

4 » Infantile ˃Also called “classic” ˃Most common » Juvenile ˃Produce small amounts of Hex A ˃Develop symptoms between ages 2 and 10 » Adult or Late Onset ˃Milder symptoms ˃Symptoms usually develop between adolescence and mid-30s ˃Do not lose hearing or vision

5 » Usually appear at 6 months to 2 years after birth » Hearing & visual problems » Loss of muscle strength » Dementia » Irritability » Loss of muscle function or paralysis » Loss of motor skills » Seizures » Slow growth » Listlessness » “Red cherry” spot in retina

6 » Observation of symptoms  screening ˃Usually used to determine if unaffected individual carries one copy of mutation » Prenatal testing ˃Used to determine if fetus carries two copies of mutated gene » Enzyme assay techniques ˃Detect individuals with lower levels of hexosaminidase A through blood tests » Mutation analysis ˃Polymerase chain reaction (PCR) obtained  amplify a sample of DNA and then test genetic markers to identify specific mutations

7 » Treatment only for alleviation of symptoms » Death usually occurs between ages 2 to 4 for infantile ˃Age 15 for Juvenile ˃Ages vary greatly for Late-Onset

8 » Autosomal recessive » Caused by defective gene on chromosome 15 » 3 types  no definitive cure

9 » “About Tay-Sachs”. Cure Tay-Sachs Foundation. Web. 7 December 2013. » “Hex A”. Genetics Home Reference. Web. 7 December 2013. » “Hexosaminidase A Deficiency”. Counsyl. Web. 7 December 2013. » “Learning About Tay-Sachs Disease”. National Human Genome Research Institute. Web. 7 December 2013. » “Tay-Sachs Disease”. Center for Jewish Genetics. Web. 7 December 2013. » “Tay-Sachs Disease”. Genetics Home Reference. Web. 7 December 2013. » “Tay-Sachs Disease”. National Tay-Sachs & Allied Diseases. Web. 7 December 2013.


Download ppt "Rachel Wells. » Warren Tay, 1881 ˃Observed symptomatic red spot in retina of eye » Bernard Sachs, 1887 ˃Described cellular changes in disease ˃Noticed."

Similar presentations


Ads by Google