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تعداد ایتم قابل مشاهده باقیمانده : 3 مورد
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Metabolic causes of hydrops

Metabolic causes of hydrops
Mucopolysaccharidosis type VII (MPS VII, Sly disease)
Mucopolysaccharidosis type IVA (MPS IVA, Morquio type A)
Mucolipidosis I (sialidosis)
Mucolipidosis II (I-cell disease)
Gaucher disease
Niemann-Pick C
Farber disease
GM1 gangliosidosis
Sialic acid storage disease
Primary carnitine deficiency
Fumarase deficiency
Respiratory chain disorders
Congenital disorders of glycosylation
Neonatal haemochromatosis
Zellweger
Glycogen storage disease type IV (GSD IV)
Deficiencies of red cell glycolytic/pentose phosphate pathway enzymes (eg, G6PDH deficiency, pyruvate kinase deficiency)
GM1: monosialotetrahexosylganglioside; G6PDH: glucose-6-phosphate dehydrogenase.
Courtesy of V Reid Sutton, MD.
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