Mucopolysaccharidosis VII as cause of fetal hydrops in early pregnancy
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference12 articles.
1. A severe infantile sialidosis: Clinical, biochemical, and microscopic features
2. Neuraminidase deficiency presenting as non-immune hydrops fetalis
3. (1992): Gml gangliosidosis Type 2 in two siblings. J Child Neurol (in press).
4. β-Glucuronidase Deficiency
5. Mucopolysaccharidosis VII (β-glucuronidase deficiency) presenting as nonimmune hydrops fetalis
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1. Clinical features of fetal hydrothorax associated with mucopolysaccharidosis‐VII;Journal of Obstetrics and Gynaecology Research;2023-07-19
2. Elevation of glycosaminoglycans in the amniotic fluid of a fetus with mucopolysaccharidosis VII;Prenatal Diagnosis;2017-03-12
3. Mucopolisacaridosis;EMC - Pediatría;2016-09
4. The Different Forms of Mucopolysaccharidosis with Neurological Involvement: A Case-Based Review;Journal of Pediatric Biochemistry;2016-04-26
5. Clinical course of sly syndrome (mucopolysaccharidosis type VII);Journal of Medical Genetics;2016-02-23
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