Literature DB >> 6839525

Clinical heterogeneity in a sibship with Niemann-Pick disease type C.

S Yatziv, Z Leibovitz-Ben Gershon, A Ornoy, G Bach.   

Abstract

The clinical presentation of Niemann-Pick type C is variable. However, in families hitherto described, the affected individuals in a given sibship show a similar clinical course. A family with histological and biochemical findings of Niemann-Pick type C is described. Four of the affected siblings presented with an early onset and a fulminant course resembling Niemann-Pick type A, whereas in the fifth sibling a later onset and a much slower neurological deterioration was observed. Genetic counseling in families with Niemann-Pick type C should take into consideration the possibility of clinical heterogeneity within the same sibship.

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Year:  1983        PMID: 6839525     DOI: 10.1111/j.1399-0004.1983.tb01860.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  3 in total

1.  Tau deletion exacerbates the phenotype of Niemann-Pick type C mice and implicates autophagy in pathogenesis.

Authors:  Chris D Pacheco; Matthew J Elrick; Andrew P Lieberman
Journal:  Hum Mol Genet       Date:  2008-12-12       Impact factor: 6.150

2.  Niemann-Pick-like liver disease and reduced cholesterol esterification in fibroblasts of two male infants.

Authors:  K Kristjansson; M J Finegold; P G Pentchev; J W Belmont
Journal:  Eur J Pediatr       Date:  1994-05       Impact factor: 3.183

Review 3.  Niemann-Pick disease type C: an update.

Authors:  M T Vanier; P Pentchev; C Rodriguez-Lafrasse; R Rousson
Journal:  J Inherit Metab Dis       Date:  1991       Impact factor: 4.982

  3 in total

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