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1 Possible Causes for Congenital Neonatal Ascites Type 2

  • Neuraminidase 1 Deficiency

    WHO-ICD-10 version:2010 Endocrine, nutritional and metabolic diseases Metabolic disorders Mode of Inheritance Autosomal recessive Gene Map Locus Neuraminidase deficiency, commonly known as sialidosis, is a lysosomal storage disorder, characterized by a deficiency of the enzyme alpha-N-acetyl neuraminidase (sialidase).[…][cags.org.ae]

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