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

Mucopolysaccharidosis type IV (MPS IV), also known as Morquio syndrome, is a progressive condition that mainly affects the skeleton. Explore symptoms, inheritance, genetics of this …

Apr 22, 2024 · Morquio syndrome, or mucopolysaccharidosis IV (MPS IV), is a genetic condition that causes symptoms like bone growth abnormalities. Symptoms occur because enzymes …

Sep 5, 2019 · Mucopolysaccharidosis IV (MPS IV) is a mucopolysaccharide storage disease that exists in two forms (MPS IVA and MPS IVB). These are autosomal recessive genetic …

MPS IV is a mucopolysaccharide disease known as Morquio or Morquio-Brailsford syndrome. MPS IV takes its name from Dr. Morquio, a pediatrician in Montevideo, Uruguay, who in 1929 …

Jul 19, 2024 · MPS IV. MPS IV (also known as Morquio syndrome) has two subtypes that result from the missing or deficient enzymes N-acetylgalactosamine-6-sulfatase (Type A) or beta …

Mucopolysaccharidosis type IV (MPS IV), also known as Morquio syndrome, is a rare metabolic condition in which the body is unable to break down long chains of sugar molecules called …

What is MPS IV? MPS IV, known as Morquio disease, is one of the mucopolysaccharide storage diseases. MPS IV disease was first identified by Dr Morquio in 1929 and includes 2 different …

Jun 23, 2017 · Maroteaux-Lamy syndrome (mucopolysaccharidosis type VI; MPS VI) is characterized by a deficiency of the enzyme N-acetylgalactosamine-4-sulfatase, resulting in …

Morquio is also known as MPS IV. In children with Morquio syndrome, the body cannot break down sugar chains called glycosaminoglycans that help build bone, cartilage, eye corneas, …