![Itebimien Peter on X: "@studyrare Hurler syndrome is a rare autosomal recessive lysosomal storage disorder usually manifests as cognitive developmental delay,corneal clouding,cardiac disease,musculoskeletal manifestations,hearing loss, recurrent ... Itebimien Peter on X: "@studyrare Hurler syndrome is a rare autosomal recessive lysosomal storage disorder usually manifests as cognitive developmental delay,corneal clouding,cardiac disease,musculoskeletal manifestations,hearing loss, recurrent ...](https://pbs.twimg.com/media/F9r7I7tW4AAHVgg.jpg)
Itebimien Peter on X: "@studyrare Hurler syndrome is a rare autosomal recessive lysosomal storage disorder usually manifests as cognitive developmental delay,corneal clouding,cardiac disease,musculoskeletal manifestations,hearing loss, recurrent ...
SP SIR - Hurler syndrome is the most severe form of mucopolysaccharidosis type-1. -It is an inherited disorder that is caused by faulty gene. -This disorder lacks the enzyme which digest the
![SciELO - Brasil - Hurler Syndrome: a Biochemically Confirmed Case in Dominican Republic Hurler Syndrome: a Biochemically Confirmed Case in Dominican Republic SciELO - Brasil - Hurler Syndrome: a Biochemically Confirmed Case in Dominican Republic Hurler Syndrome: a Biochemically Confirmed Case in Dominican Republic](https://minio.scielo.br/documentstore/2326-4594/GmRSV3CXFTSbWv6T4ZNCFNy/d690a77317c62f7c651c9237bdf155d046c0479f.jpg)