HISTOPATHOLOGICAL DIAGNOSIS OF A TYPE VII MUCOPOLYSACCHARIDOSIS AFTER PREGNANCY TERMINATION

Abstract

Type VII mucopolysaccharidosis is a very rare recessive lysosomal storage disease. We diagnosed a type VII MPS in a case of severe fetal hydrops after pregnancy termination at 23 weeks of gestation. The diagnosis was suspected on histopathological examination by the presence of foam cells in many viscera and foamy placental Hofbauer cells. Enzyme assay on cultured amniotic cells showed a markedly deficient β-glucuronidase activity, thus confirming the diagnosis. This report shows the importance of a precise necropsy diagnosis in nonimmune hydrops because of putative implications for genetic counseling and prenatal diagnosis in subsequent pregnancies.

Keywords:

• β-glucuronidase deficiency
• mucopolysaccharidosis
• nonimmune fetal hydrops
• prenatal diagnosis