Literature DB >> 3146334

Placental pathology and prenatal diagnosis of infantile type of neuronal ceroid-lipofuscinosis.

J Rapola1, P Santavuori, H Heiskala.   

Abstract

Five term placentae from pregnancies at risk of infantile neuronal ceroid-lipofuscinosis (INCL) were studied electron-microscopically to determine if diagnostic cytoplasmic inclusions could be detected in this tissue. In 4 placentae no inclusions were found, and the infants born from these pregnancies have developed normally, the shortest observation time being 15 months. In the fifth placenta numerous cytosomes pathognomonic of INCL were found in the amniotic cells and the endothelium of the capillaries of the chorionic villi. The diagnostic significance of this finding was confirmed by the presence of typical inclusions in the autonomic ganglion cells and other cells in a rectal mucosal biopsy specimen of this male infant at the age of 3 months. Electron microscopic study of chorionic villus biopsy specimens appears to be a promising possibility for prenatal diagnosis of INCL.

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Year:  1988        PMID: 3146334     DOI: 10.1002/ajmg.1320310613

Source DB:  PubMed          Journal:  Am J Med Genet Suppl        ISSN: 1040-3787


  1 in total

1.  Prenatal diagnosis of infantile neuronal ceroid-lipofuscinosis, INCL: morphological aspects.

Authors:  J Rapola; R Salonen; P Ammälä; P Santavuori
Journal:  J Inherit Metab Dis       Date:  1993       Impact factor: 4.982

  1 in total

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