Concluded Case

HUNTER'S SYNDROME

Good evening dear friends and fellow colleagues, Today let us have a look at HUNTER'S SYNDROME also known as MUCO POLYSACCHARIDOSIS type II. This is a rare , inherited disorder in which the body doesn't properly digest sugar molecules in the body due to deficiency of a enzyme Iduronate 2 Sulfatase. When these molecules build up in the organs and tissues overtime , they can cause damage that affects physical and mental development and abilities. This disorder almost always occurs in boys . There is no cure . With regards, Dr Sepuri Tirumala Devi.

5 Likes

LikeAnswersShare
Concluded answer
A really complete and illustrative description of HUNTER'S SYNDROME- an X - linked recessive disorder. Never got opportunity to come across a case of hunter's syndrome. But this a a complete description and informative- Thanks
All Answers
A really complete and illustrative description of HUNTER'S SYNDROME- an X - linked recessive disorder. Never got opportunity to come across a case of hunter's syndrome. But this a a complete description and informative- Thanks
Thank you doctor
0
Elaborate and descriptive post about HUNTER SYNDROME THANX MAM
Thanx dr Manoja Raulo
0

View 4 other replies

Nicely illustrated Madam Thanks for sharing
Thank you doctor
0
Nice briefing Mam
Thank you doctor
0
Good info
Thank you doctor
0
Thanks doctors for giving a informative knowledge of rare of the rarest case.
Thank you doctor
0
SUGGESTIVE of NICE UPDATE... USEFUL AND INFORMATIVE
Again a nice case is represented by u mam!
Thank you doctor
0
Very informative post mam
Thank you Dr Nikhat sajjad
0
Very lucid presentation
Thank you doctor
0
Load more answers

Cases that would interest you