Mucopolysaccharidosis type VII as a cause of recurrent non-immune hydrops fetalis
Author:
Publisher
Walter de Gruyter GmbH
Subject
Obstetrics and Gynaecology,Pediatrics, Perinatology, and Child Health
Link
https://www.degruyter.com/document/doi/10.1515/JPM.2003.083/pdf
Reference7 articles.
1. In-utero diagnosis of mucopolysaccharidosis type VII in a fetus with an enlarged nuchal translucency
2. Mucopolysaccharidosis VII (Sly disease) as a cause of increased nuchal translucency and non-immune fetal hydrops: study of a family and technical approach to prenatal diagnosis in early and late pregnancy
3. β-glucuronidase deficiency as a cause of fetal hydrops
4. Mucopolysaccharidosis VII as cause of fetal hydrops in early pregnancy
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1. Atypical Neuroimaging Findings in a Patient With Mucopolysaccharidosis Type VII (Sly Syndrome);Cureus;2024-08-13
2. Mucopolysaccharidosis VII in Brazil: natural history and clinical findings;Orphanet Journal of Rare Diseases;2021-05-22
3. Exome Sequencing for Prenatal Diagnosis in Nonimmune Hydrops Fetalis;New England Journal of Medicine;2020-10-29
4. Relevance of the Materno-Fetal Interface for the Induction of Antigen-Specific Immune Tolerance;Frontiers in Immunology;2020-05-14
5. Otorhinolaryngological Findings in Patients from Southwestern Colombia with Clinical, Enzymatic and Molecular Diagnosis of Mucopolysaccharidosis II, IV-A and VI;Journal of Inborn Errors of Metabolism and Screening;2020
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