Clinical and Radiological Characterisation of Patients with Mucopolysaccharidosis in a Genetic Clinic
Abstract The mucopolysaccharidoses (MPS) are a relatively uncommon group of inherited metabolic disorders. MPSs should be suspected in a child with coarse facies, organomegaly, recurrent respiratory tract infections, developmental delay, and hernias. Early diagnosis and treatment can greatly improve...
| Main Authors: | , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
SciELO
2021-03-01
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| Series: | Journal of Inborn Errors of Metabolism and Screening |
| Subjects: | |
| Online Access: | http://www.scielo.br/scielo.php?script=sci_arttext&pid=S2326-45942021000100503&tlng=en |