Mucopolysaccharidosis type 4 natural cures

Mucopolysaccharidosis type 4 Definition

This is also known as Morqui syndrome, a disorder known to be autosomal recessive mucopolysaccharide disease that is usually inherited. It is also considered somewhat a rare case of dwarfism with serious consequences. This happens when the body is unable process certain types of mucopplysaccharides, then they just build up or are eliminated causing a range of symptoms. The type A form is a deficiency of the enzyme N-acetylgalactosamine-6-sulfate sulfatase.

Mucopolysaccharidosis type 4 Diagnosis

Unusual curvature of the spine or kyphoscoliosis, cloudy cornea, heart murmur, inquinal hernia, liver enlargement, loss of nerve function below the neck and short stature may be revealed through a physical examination. Blood culture, echocardiogram, genetic testing, hearing test, slit-lamp eye exam, skin fibrolast culture and x-rays of the long bones, ribs and spine are also possible tests.

Mucopolysaccharidosis type 4 Treatment

Now, only soothing measures are available to treat Morquio syndrome patients. Physicians normally recommend cervical spine fusion to patients since all of those with the disorder have odontoid hypoplasia that can lead to atlanoaxial subluxation.

Mucopolysaccharidosis type 4 Symptoms and Signs

Morquio syndrome has an several symptoms and among them are abnormal heart development, abnormal skeletal development, hypermobile joints, large fingers, knock-knees, widely spaced teeth, large head, bell shaped chest, compression of spinal cord, enlarged heart, and dwarfism.

Mucopolysaccharidosis type 4 Causes
Type A of this Mucopolysaccharidosis is caused by a deficiency of the enzyme N-acetylgalactosamine-6-sulfate sulfatase while type B is caused by a deficiency of the enzyme beta-galactosidase.


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