Literature DB >> 2735192

Adult-type citrullinemia.

R Okeda1, M Tanaka, Y Kawahara, J Tokushige, T Imai, K Kameya.   

Abstract

An autopsy case of adult-type citrullinemia in a 42-year-old male is reported. The patient neuropathologically presented mixed cerebral changes consisting of the pseudoulegyric and ischemic types of hepatocerebral disease. In common with previously reported cases of the pseudoulegyric type, the nature and localization of the cerebral changes in this case were characteristic, in that neuronal loss occurred most severely and symmetrically in the mediobasal part of the frontal and occipital lobes, gyrus cinguli, claustrum, insula and temporal lobe, and that the watershed area of the cerebral cortex, basal ganglia and Purkinje cells were only slightly affected. The importance of hypercitrullinemia was stressed in the pathogenesis of the cerebral changes evident in adult-type citrullinemia.

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Mesh:

Year:  1989        PMID: 2735192     DOI: 10.1007/bf00687408

Source DB:  PubMed          Journal:  Acta Neuropathol        ISSN: 0001-6322            Impact factor:   17.088


  12 in total

1.  [A HEPATOCEREBRAL DISEASE AUTOPSY CASE HAVING WIDESPREAD INCOMPLETE CORTICAL NECROSIS ("ERBLEICHUNG"), MAKING A SPECIAL REFERENCE TO THE SO-CALLED PSEUDOULEGYRIA TYPE (SHIRAKI)].

Authors:  S ANDO; Y OHSHIMA; K URYU
Journal:  Seishin Shinkeigaku Zasshi       Date:  1964-06

2.  [An autopsied case of the "pseudoulegyria type" of the hepatocerebral disease].

Authors:  H SHIRAKI; T YAMAMOTO; K YAMADA; T SHIKATA
Journal:  Seishin Shinkeigaku Zasshi       Date:  1962-03

3.  A vulnerable and rate-limiting step in urea synthesis in patients with hyperammoniaemia.

Authors:  D C PEARL; W V McDERMOTT
Journal:  Proc Soc Exp Biol Med       Date:  1958-02

4.  A variant form of citrullinemia.

Authors:  I Matsuda; M Anakura; S Arashima; Y Saito; Y Oka
Journal:  J Pediatr       Date:  1976-05       Impact factor: 4.406

5.  [An autopsy case of juvenile hepato-cerebral degeneration (non-Wilsonian Inose-type) with mental retardation, with special reference to ammonia and amino acids metabolism (author's transl)].

Authors:  M Takamizawa; M Toru; T Kojima; A Watanabe; K Hirokawa
Journal:  Seishin Shinkeigaku Zasshi       Date:  1973-06

6.  Neuropathology of citrullinaemia.

Authors:  J J Martin; J P Farriaux; P De Jonghe
Journal:  Acta Neuropathol       Date:  1982       Impact factor: 17.088

7.  Enzymatic analysis of citrullinemia (12 cases) in Japan.

Authors:  T Saheki; A Ueda; M Hosoya; M Sase; K Nakano; T Katsunuma
Journal:  Adv Exp Med Biol       Date:  1982       Impact factor: 2.622

8.  Distribution of cerebral lesions in acquired hepatocerebral degeneration.

Authors:  M H Finlayson; B Superville
Journal:  Brain       Date:  1981-03       Impact factor: 13.501

9.  Citrullinemia.

Authors:  J Leibowitz; J Thoene; E Spector; W Nyhan
Journal:  Virchows Arch A Pathol Anat Histol       Date:  1978-03-10

10.  Neonatal type of argininosuccinate synthetase deficiency. Report of two cases with autopsy findings.

Authors:  H Kuhara; T Wakabayashi; H Kishimoto; K Hayashi; T Katoh; J Itoh; Y Wada
Journal:  Acta Pathol Jpn       Date:  1985-07
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  1 in total

1.  CT findings in the infantile form of citrullinemia.

Authors:  Sait Albayram; Kieran J Murphy; Philippe Gailloud; Abhay Moghekar; James A Brunberg
Journal:  AJNR Am J Neuroradiol       Date:  2002-02       Impact factor: 3.825

  1 in total

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