The clinical and genotypic–phenotypic findings of mucopolysaccharidosis VI patients: an Iraqi single-study descriptive study

BACKGROUND: Maroteaux–Lamy syndrome (mucopolysaccharidosis type VI; MPS VI) is a chronic illness that causes progressive enlargement, inflammation, or scarring of several tissues and organs until their collapse. In most cases, an infant with MPS VI shows no symptoms. The early signs and symptoms of...

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Detalles Bibliográficos
Autores principales: Baheer Abdul Wahhab, Saja, Farhan Thejeal, Rabab, Swed, Sarya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2023
Materias:
Original Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10553017/
https://www.ncbi.nlm.nih.gov/pubmed/37811045
http://dx.doi.org/10.1097/MS9.0000000000001272

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10553017/
https://www.ncbi.nlm.nih.gov/pubmed/37811045
http://dx.doi.org/10.1097/MS9.0000000000001272

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