Cardiology · Cardiology / Genetic cardiology
Maroteaux–Lamy syndrome
also: Mucopolysaccharidosis type VI
Lysosomal storage disease with valve thickening and normal intelligence.
- Specialty
- Cardiology
- Subspecialty
- Cardiology / Genetic cardiology
- Sex & age distribution
- Male: affected; Female: affected equally; Children: yes
- Gene(s) involved
- ARSB
- Alternative names & eponyms
- Mucopolysaccharidosis type VI
Etiology & mechanism
ARSB deficiency.
Gene(s) involved (1)
Symptoms & signs (6)
In plain terms, someone with Maroteaux–Lamy syndrome may experience the following — click any to explore related syndromes:
Same gene(s)
Other syndromes that involve one of this syndrome's genes.
Overlapping symptoms
Other syndromes that share symptoms with this one.
Drag nodes, scroll to zoom, click a node to open that syndrome.
Shares symptoms with
3 shared
Hurler syndrome
corneal clouding, hepatosplenomegaly, valve thickening
3 shared
Scheie syndrome
corneal clouding, joint stiffness, normal intelligence
2 shared
3M syndrome
normal intelligence, short stature
2 shared
Hunter syndrome
hepatosplenomegaly, short stature
2 shared
Hurler–Scheie syndrome
corneal clouding, joint stiffness
2 shared
Morquio syndrome
corneal clouding, normal intelligence
1 shared
Aarskog–Scott syndrome
short stature
1 shared
Andersen–Tawil syndrome
short stature
1 shared
Antiphospholipid syndrome cardiac manifestations
valve thickening
1 shared
Bloom syndrome
short stature
Shares genes with
None.
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