Literature DB >> 1149307

The pathological anatomy of the Smith-Lemli-Opitz syndrome.

E D Cherstvoy, G I Lazjuk, I W Lurie, M K Nedzved, S S Usoev.   

Abstract

Two cases of the Smith-Lemli-Opitz syndrome are described, together with the autopsy findings. In both cases, the typical appearance and visceral malformations were present. Hypoplasia of the frontal lobes and corpus callosum, and aplasia of the splenium constitute abnormalities of the brain which may be useful in the diagnosis of this disorder at autopsy. The autosomal recessive mode of inheritance of this syndrome was confirmed.

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Year:  1975        PMID: 1149307     DOI: 10.1111/j.1399-0004.1975.tb00345.x

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


  6 in total

1.  Unknown syndrome: ischiadic hypoplasia, renal dysfunction, immunodeficiency, and a pattern of minor congenital anomalies.

Authors:  C Braegger; A Bottani; F Hallé; A Giedion; E Leumann; R Seger; U Willi; A Schinzel
Journal:  J Med Genet       Date:  1991-01       Impact factor: 6.318

2.  Autism as a sequence: from heterochronic germinal cell divisions to abnormalities of cell migration and cortical dysplasias.

Authors:  Manuel F Casanova
Journal:  Med Hypotheses       Date:  2014-04-13       Impact factor: 1.538

Review 3.  The Smith-Lemli-Opitz syndrome.

Authors:  R I Kelley; R C Hennekam
Journal:  J Med Genet       Date:  2000-05       Impact factor: 6.318

4.  The Smith-Lemli-Opitz syndrome. A detailed pathological study as a clue to a etiological heterogeneity.

Authors:  E D Cherstvoy; G I Lazjuk; T I Ostrovskaya; I A Shved; G I Kravtzova; I W Lurie; A I Gerasimovich
Journal:  Virchows Arch A Pathol Anat Histopathol       Date:  1984

5.  Brain magnetic resonance imaging findings in Smith-Lemli-Opitz syndrome.

Authors:  Ryan W Y Lee; Sandra K Conley; Andrea Gropman; Forbes D Porter; Eva H Baker
Journal:  Am J Med Genet A       Date:  2013-08-05       Impact factor: 2.802

Review 6.  Lethal acrodysgenital dwarfism: a severe lethal condition resembling Smith-Lemli-Opitz syndrome.

Authors:  M L Merrer; M L Briard; S Girard; N Mulliez; C Moraine; M C Imbert
Journal:  J Med Genet       Date:  1988-02       Impact factor: 6.318

  6 in total

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