experience severe mucopolysaccharidosis type I, while approximately 1 in 500,000 newborns will experience attenuated mucopolysaccharidosis type I. Most...

Sanfilippo syndrome, also known as mucopolysaccharidosis type III (MPS III), is a rare lifelong genetic disease that mainly affects the brain and spinal...

[citation needed] All members of the mucopolysaccharidosis family are also lysosomal storage diseases. Mucopolysaccharidosis type I (MPS I) is divided into...

Hunter syndrome, or mucopolysaccharidosis type II (MPS II), is a rare genetic disorder in which large sugar molecules called glycosaminoglycans (or GAGs...

Maroteaux–Lamy syndrome, or Mucopolysaccharidosis Type VI (MPS-VI), is an inherited disease caused by a deficiency in the enzyme arylsulfatase B (ARSB)...

Mucopolysaccharidosis type I is a spectrum of diseases in the mucopolysaccharidosis family. It results in the buildup of glycosaminoglycans (or GAGs,...

Sly syndrome, also called mucopolysaccharidosis type VII (MPS-VII), is an autosomal recessive lysosomal storage disease caused by a deficiency of the...

Morquio syndrome, also known as mucopolysaccharidosis type IV (MPS IV), is a rare metabolic disorder in which the body cannot process certain types of...

Dermatology. Saunders Elsevier. ISBN 978-0-7216-2921-6. "Mucopolysaccharidosis". "MUCOPOLYSACCHARIDOSIS, TYPE IX;MPS9". "Mucopolysaccharidoses - Symptoms, Causes...

Mucolipidosis type 4 Mucopolysaccharidosis type 3 Mucopolysaccharidosis type 4 Mucopolysaccharidosis type I Hurler syndrome Mucopolysaccharidosis type I Hurler/Scheie...

glycosylation MOMO syndrome Mucopolysaccharidosis type 6 Mucopolysaccharidosis type 7 Mucopolysaccharidosis, MPS-II Mucopolysaccharidosis, MPS-III-D Muenke syndrome...

type 3 Mucopolysaccharidosis type 6 Mucopolysaccharidosis type 7 Sly syndrome Mucopolysaccharidosis type I Hurler syndrome Mucopolysaccharidosis type I...

deficiency of the enzyme iduronidase.[citation needed] All forms of mucopolysaccharidosis type I (MPS I) are a spectrum of the same disease. Hurler-Sheie...

glycosaminoglycans (GAGs) in the body. It is the most mild subtype of mucopolysaccharidosis type I; the most severe subtype of this disease is called Hurler...

the United States Hurler syndrome, genetic disorder also known as mucopolysaccharidosis type I (MPS I), Hurler's disease, or gargoylism The Hurlers (stone...

(MPS) constitute a commonly seen group of osteochondrodysplasias. Mucopolysaccharidosis can cause a wide spectrum of clinical and radiologic manifestations...

recessive inherited metabolic disease known as Sly syndrome or Mucopolysaccharidosis VII. A deficiency in this enzyme results in the build-up of non-hydrolyzed...

(also called mucopolysaccharidosis type VI) Iduronidase (branded as Aldurazyme), a recombinant protein therapeutic for mucopolysaccharidosis I Amifampridine...

an enzyme replacement therapy (Aldurazyme) for the rare disorder Mucopolysaccharidosis (MPS I). The struggle to get the therapy translated from a successful...

4-sulfate sulfohydrolase, EC 3.1.6.12) is an enzyme associated with mucopolysaccharidosis VI (Maroteaux–Lamy syndrome). Arylsulfatase B is among a group of...

nuclear type 20 Mitochondrial complex III deficiency nuclear type 7 Mucopolysaccharidosis, MPS-III-A to -D Neurodevelopmental disorder with dysmorphic facies...

lead to serious diseases as noted below. Sanfillipo Syndrome or Mucopolysaccharidosis III, MPS III, is a lysosomal storage disease resulting from a deficiency...

original on 2013-08-13. Retrieved 2012-06-27. Skipperke Club, p. 2 "Mucopolysaccharidosis (MPS) IIIB". UPenn School of Veterinary Medicine. "New DNA-based...

α-glucosidase. Hers also suggested that other diseases, such as the mucopolysaccharidosis, might be due to enzyme deficiencies.[citation needed] Mannosidosis...

to progressing clinical research into the effective treatment of Mucopolysaccharidosis III, also known as MPSIII or Sanfilippo Syndrome. The song peaked...

gene that result in enzymatic deficiency lead to the sex-linked mucopolysaccharidosis type II, also known as Hunter syndrome. At least 174 disease-causing...

syndromic 12 Miller syndrome Mohr syndrome Mucolipidosis type II Mucopolysaccharidosis, MPS-I-H/S Multiple congenital anomalies-hypotonia-seizures syndrome...

is an inherited abnormality of white blood cells associated with mucopolysaccharidosis. When blood smears and bone marrow preparations from patients with...

Macroglossia may be a sign of hypothyroid disorders. Other causes include mucopolysaccharidosis, neurofibromatosis, multiple endocrine neoplasia type 2B, myxedema...

deficiency is the cause of the lysosomal storage disease called mucopolysaccharidosis type VII. Congenital disorders of glycosylation Parvovirus B19 (fifth...