Mucopolysaccharidosis type III (Sanfilippo syndrome) and misdiagnosis of idiopathic developmental delay, attention deficit/hyperactivity disorder or autism spectrum disorder

Mucopolysaccharidosis III is a rare genetic disease characterized by progressive cognitive decline and severe hyperactivity that does not respond to stimulants. Somatic features are relatively mild. Patients are often initially misdiagnosed as having idiopathic developmental delay, attention deficit...

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Detalles Bibliográficos
Autores principales: Wijburg, Frits A, Węgrzyn, Grzegorz, Burton, Barbara K, Tylki-Szymańska, Anna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2013
Materias:
Review Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3654162/
https://www.ncbi.nlm.nih.gov/pubmed/23336697
http://dx.doi.org/10.1111/apa.12169

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3654162/
https://www.ncbi.nlm.nih.gov/pubmed/23336697
http://dx.doi.org/10.1111/apa.12169

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