Disorders of glycosaminoglycan metabolism | Medibuddy
5th February 2024

Disorders of glycosaminoglycan metabolism

Pathophysiology

Glycosaminoglycans, or mucopolysaccharides, are the degradation products of proteoglycans in the extracellular matrix and are proteolytic cleaved, giving origin to GAGs, which enter the lysosome for intracellular digestion. There are four different pathways:

  • Dermatan sulfate
  • Heparan sulfate
  • Keratan sulfate
  • Chondroitin sulfate

Mucopolysaccharidoses (MPs) are a group of inherited lysosomal storage disorders in which the abnormal accumulation of specific carbohydrate complexes can cause chronic and progressive symptoms with varying severity. Features can include organomegaly, dysostosis multiplex and characteristic abnormal facies. Definitive diagnosis is enzymatic assays of the defective enzyme in cultured fibroblasts, leucocytes, and serum or plasma. MPs are inherited in an autosomal recessive fashion, except MPS II (Hunter syndrome), which is X-linked.

Clinical summary

The table below shows details of common mucopolysaccharidoses that are favourites in the MRCP Part 1 exam:

Group Syndrome Deficiency Accumulation Features
MPS 1-H;S;H/S Hurler syndrome Alpha-L-iduronidase Dermatan sulfates

Heparan sulfates

Most severe form

Developmental delays

Recurrent urinary and respiratory tract infections, skeletal deformities,

Cloudy cornea, pigmentary retinopathy

cheie syndrome Alpha-L-iduronidase Dermatan sulfate Mildest form

Normal IQ, height and life expectancy

Stiff joints, aortic regurgitation, cloudy cornea

Hurler-Scheie syndrome Alpha-L-iduronidase Dermatan sulfate Severity in-between Hurler and Scheie syndrome

Coarse facial features, joint stiffness, cloudy corneas, hepatosplenomegaly, skeletal and cardiac abnormalities

MPS II Hunter syndrome Iduronate sulfatase Dermatan sulfate

Heparan sulfate

Progressive growth delays, short stature, stiff joints

Macrocephaly, hepatosplenomegaly

IIA (more severe form)- reduced IQ

IIB (mild form)- normal IQ

Cornea is clear

MPS III Sanfilippo syndrome Heparan N-sulfatase Heparan sulfate Four subtypes (A, B, C, D)

Hyperactivity, sleep disorders, varying intellectual disability, seizures, unsteady gait

Pigmentary retinopathy and optic atrophy

MPS IV Morquio syndrome N-acetyl-galactosamine-6-sulfatase and beta galactosidase Keratan sulfate

Chondroitin sulfate

Normal IQ

Skeletal dysplasia

Prominent lower face, abnormally short neck, genu valgum, flat feet, kyphoscoliosis

Cloudy cornea

MPS VI Maroteaux-Lamy syndrome N-acetylgalactosamine-4-sulfatase Dermatan sulfate Normal IQ

Coarse facial features, umbilical hernia, joint contractures, hepatosplenomegaly

Cloudy cornea

MPS VII Sly syndrome Beta-glucuronidase Dermatan sulfate

Heparan sulfate

Chondroitin sulfate

Normal IQ

Skeletal/facial dysmorphism

Cloudy cornea

Hydrocephalus, short stature, heart diseases

Hydrops fetalis

References

Coutinho MF, Lacerda L, Alves S. Glycosaminoglycan storage disorders: a review. Biochemistry research international. 2012 Oct;2012.

Mobile app screenshots

Take your subscriptions with you

Our mobile app allows you to access your interview and exam question banks wherever you are.