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SpringsofIyore — hannahslion: Connor
Published: 2011-10-15 01:50:15 +0000 UTC; Views: 226; Favourites: 3; Downloads: 1
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Description
Name: ConnorGender: XY
Markings: Coloured Mane, Coloured Tail, Floe Spots
Custom - Dark Orange Marks
Conditions: Tell me a fact about MPSIIa.
*Edit - There does not appear to be a lot of information on MPSIIa, which is the more acute side of the MPSII. I will take a fact on MPSII.
- If you can be the first to find me a fact on MPSIIa (even if this guy has been claimed) I will make you another orange lhedis. <3
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How To Adopt: [link]
All Creatures belong to *Cao
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Comments: 21
It's known as Hunter syndrome, and MPSIIa is an early onset version, some symptoms including a broad nose with flared nostrils, an early decline in developmental skills (ages 1.5-3), claw like hands, and skeletal irregularities.
Claim: TBN
By the way, is this what your brother had?
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hannahslion beat you to this one, but I will make another one for you for getting me a MPSIIa fact.
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Thanks. And I'm so sorry for your loss. It's great that you're doing things like this though, or I wouldn't know anything about that disease.
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Most of the doctors we saw at the Children's Hospital throughout his life had never heard of it either. D: It's a very rare disease.
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It seems so! But doing this has certainly spread the word about it, even if it's only to a few people. I also saw that you have a group on MPS on your main account. I think it's wonderful that you're doing things to fight the disease <3
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WAIT! this one
Claim: Neanderthal
(info from [link])
I think its stands for Sanfilippo syndrome which is a rare " autosomal recessive lysosomal storage disease" caused by the enzymes needed to break down glycosaminoglycan heparan sulfate.
Types A,B,C and D are basically indistinguishable and is a mutation in the genes
i think...
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No, I'm sorry. That is also about MPSIII.
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ok
Well I got the avis so im happy
And I'm sorry about your brother <3
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(info from [link] )
I think its stands for Sanfilippo syndrome which is a rare " autosomal recessive lysosomal storage disease" caused by the enzymes needed to break down glycosaminoglycan heparan sulfate.
Types A,B,C and D are basically indistinguishable and is a mutation in the genes
i think...
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The condition is named for Sylvester Sanfilippo, the pediatrician who first described the disease.
claim: Sylvester
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No, I'm sorry, that's MPSIII.
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Early-onset Hunter syndrome (MPS IIA) is the more common and more severe of the two types and usually appears around age 2 and up to age 4.
Its for your brother isnt it?
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Also, do you still want the name Sylvester?
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LOL cao, I wanted Flitter for the Favorite raffle XD this one i actualy wanna change my mind about, I wanna name him Connor <3
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In honor of your brother.
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I had just sent you a note about that. XD
And thank you, it's great honour. <3
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