Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/55962
Type: Journal article
Title: Prosaposin deficiency - a rarely diagnosed, rapidly progressing, neonatal neurovisceral lipid storage disease. Report of a further patient
Author: Elleder, M.
Jerabkova, M.
Befekadu, A.
Hrebicek, M.
Berna, L.
Ledvinova, J.
Hulkova, H.
Rosewich, H.
Schymik, N.
Paton, Barbara Cleland
Harzer, K.
Citation: Neuropediatrics, 2005; 36(3):171-180
Publisher: Georg Thieme Verlag
Issue Date: 2005
ISSN: 0174-304X
School/Discipline: School of Paediatrics and Reproductive Health : Paediatrics
Statement of
Responsibility: 
Elleder, M; Jerábková, M; Befekadu, A; Hrebícek, M; Berná, L; Ledvinová, J; Hůlková, H; Rosewich, H; Schymik, N; Paton, BC. and Harzer, K.
Abstract: An infant presented with multifocal myoclonus and cyanotic hypoxemia immediately after birth, and severe feeding problems, a protein-losing enteropathy, massive ascites and grand-mal epilepsy marked his rapid downhill course, with death at 17 weeks. At 2 weeks, brain MRI revealed grey matter heterotopias in the parieto-occipital regions suggestive of a cortical morphogenetic disorder. In cultured skin fibroblasts, lipid storage and reduced activities of ceramidase, galactosylceramide beta-galactosidase and glucosylceramide beta-glucosidase were evident. Autopsy disclosed generalised lysosomal lipid storage with macrophages and adrenal cortex prominently affected. The pattern of stored lipids in cultured fibroblasts and in dewaxed spleen tissue blocks was compatible with a diagnosis of prosaposin (pSap) deficiency (pSap-d). Neuropathologically, there was a pronounced generalised neurolysosomal storage combined with a severe depletion of cortical neurons and extreme paucity of myelin and oligodendroglia. This pathology, in particular the massive neuronal loss, differed from that in other neurolipidoses and could be explained by the reduced hydrolysis of multiple sphingolipids and the loss of pSap's neurotrophic function. The absence of immunostainable saposins on tissue sections and the presence of a homozygous c.1 A > T mutation in the prosaposin gene confirmed the diagnosis. PSap-d may be an underdiagnosed condition in infants with severe neurological and dystrophic signs starting immediately after birth.
RMID: 0020092138
Description (link): http://www.ncbi.nlm.nih.gov/pubmed/15944902
Appears in Collections:Paediatrics publications

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