-
Maroteaux–Lamy syndrome, or
mucopolysaccharidosis Type VI (MPS-VI), is an
inherited disease caused by a
deficiency in the
enzyme arylsulfatase B (ARSB)...
-
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...
-
Apert syndrome is a form of acrocephalosyndactyly, a
congenital disorder characterized by
malformations of the skull, face,
hands and feet. It is classified...
-
activist with
Maroteaux-Lamy
syndrome living in the
United States under deferred action.
Bueso was born in Guatemala. She was
diagnosed with
Maroteaux-Lamy syndrome...
- may not live
beyond their twenties or thirties.
Children with MPS VI,
Maroteaux–Lamy syndrome,
usually have
normal intellectual development but share...
-
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):...
- 20505.57. PMID 15302781. Mon****ier L,
Laplante MA, Jaffré F,
Bousquet P,
Maroteaux L, de
Champlain J (Aug 2008). "Serotonin 5-HT(2B)
receptor blockade prevents...
-
chromosome 15
syndrome Maroteaux–Cohen–Solal–Bonaventure
syndrome Maroteaux–Fonfria
syndrome Maroteaux–Le Merrer–Bensahel
syndrome Maroteaux–Stanescu–Cousin...
