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Maroteaux–Lamy syndrome, or
Mucopolysaccharidosis Type VI (MPS-VI), is an
inherited disease caused by a
deficiency in the
enzyme arylsulfatase B (ARSB)...
-
chromosome 15
syndrome Maroteaux–Cohen–Solal–Bonaventure
syndrome Maroteaux–Fonfria
syndrome Maroteaux–Le Merrer–Bensahel
syndrome Maroteaux–Stanescu–Cousin...
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Osteogenesis imperfecta (IPA: /ˌɒstioʊˈdʒɛnəsɪs ˌɪmpɜːrˈfɛktə/; OI),
colloquially known as
brittle bone disease, is a
group of
genetic disorders that all...
- An osteochondrodysplasia, or
skeletal dysplasia, is a
disorder of the
development of bone and cartilage.
Osteochondrodysplasias are rare diseases. About...
-
Genetic studies indicate that the
mutation at
chromosome 9p13-12, for AMD
Maroteaux, is a gene that
codes for a
protein that
affects bone development, natriuretic...
- Ther Nucl Med. 99 (3): 724–35. doi:10.2214/ajr.99.3.724. PMID 6020652.
Maroteaux P,
Malamut G (1968). "[Acrodysostosis]".
Presse Med (in French). 76 (46):...
- may not live
beyond their twenties or thirties.
Children with MPS VI,
Maroteaux–Lamy syndrome,
usually have
normal intellectual development but share...
- in 1995 in Elmhurst, Illinois. He was
diagnosed at the age of one with
Maroteaux–Lamy syndrome,
which in his case
resulted in
developing an appearance...
-
Apert syndrome is a form of acrocephalosyndactyly, a
congenital disorder characterized by
malformations of the skull, face,
hands and feet. It is classified...
-
syndrome (MPS II)
Sanfilippo syndrome (MPS III)
Morquio syndrome (MPS IV)
Maroteaux–Lamy
syndrome (MPS VI)
James WD,
Berger TG, et al. (2006). Andrews' Diseases...
