Click for new scientific resources and news about Corona[COVID-19]

Paper Information

Journal:   IRANIAN JOURNAL OF CHILD NEUROLOGY (IJCN)   FALL 2012 , Volume 6 , Number 4 (SUPPL 1); Page(s) 5 To 5.
 
Paper: 

MUCOPOLYSACCHARIDOSIS TYPE 1

 
 
Author(s):  ALAEE MOHAMMAD REZA*
 
* MOFID CHILDREN HOSPITAL, SHAHID BEHESHTI UNIVERSITY OF MEDICAL SCIENCES (SBMU), TEHRAN, IRAN
 
Abstract: 

Mucopolysaccharidosis (MPS) are a group of lysosomal storage disorders caused by deficiency of alfa-L-idorinidase. MPS is a progressive multisystem tissue and organ dysfunction, including cardiac, respiratory, musculoskeletal and visceral manifestations.
MPS 1 divided into three clinical phenotype: Hurler, Hurler-Scheie, Scheie syndromes.

 
Keyword(s): MUCOPOLYSACCHARIDOSIS 1, CHILD, DIAGNOSIS, THERAPY
 
References: 
  • ندارد
 
  pdf-File tarjomyar Yearly Visit 54
 
Latest on Blog
Enter SID Blog