| Autor: |
Kimberly Baez-Nicodemo, Isi Ortiz, Noemi Acevedo |
| Jazyk: |
angličtina |
| Rok vydání: |
2023 |
| Předmět: |
|
| Zdroj: |
Journal of Inborn Errors of Metabolism and Screening, Vol 11 (2023) |
| Druh dokumentu: |
article |
| ISSN: |
2326-4594 |
| DOI: |
10.1590/2326-4594-jiems-2022-0008 |
| Popis: |
Abstract Mucopolysaccharidosis (MPS) is a group of metabolic disorders caused by the deficiency or complete absence of certain lysosomal enzymes responsible for the breakdown of mucopolysaccharides, causing an accumulation of glycosaminoglycans (GAGs) throughout the body. Mucopolysaccharidosis type I (MPS I), also called Hurler syndrome, is an autosomal recessive lysosomal storage disorder resulting from a deficiency of the enzyme α-L-iduronidase. This report aims to present the clinical findings and diagnosis of a 21-month-old female with no history of similar cases in their previous generations. The diagnosis was considered based on the clinical and radiological characteristics of Hurler syndrome (HS) and confirmed biochemically, becoming the first confirmed case in the Dominican Republic. |
| Databáze: |
Directory of Open Access Journals |
| Externí odkaz: |
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