Literature DB >> 1258607

Neuropathological considerations in cerebro-hepato-renal syndrome (Zellweger's syndrome).

H M Liu, B S Bangaru, J Kidd, J Boggs.   

Abstract

The nervous system in patients with cerebro-hepato-renal syndrome appeared to be affected at various tissue levels. There was evidence of a migrational disorder manifested by polymicrogyria and lack of normal neuronal maturation. There was dysmyelination of the white matter associated with accumulation of neutral fat in astrocytes. Within the peripheral nerves, masses of tangled neurofilaments producing dystrophic axons were demonstrated by electron microscopy. These findings could be explained on the basis of a genetic metabolic defect, one that involved particularly the amino acids. The defect may have interfered with the normal intercellular reaction during embryogenesis resulting in the malformation of multiple organs. The same metabolic abnormality could have caused the hepatic damage and disturbance in normal myelination during the neonatal period.

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Year:  1976        PMID: 1258607     DOI: 10.1007/BF00684662

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


  24 in total

1.  Cerebro-hepato-renal syndrome of Zellweger. A report of eight cases with comments upon the incidence, the liver lesion, and a fault in pipecolic acid metabolism.

Authors:  D M Danks; P Tippett; C Adams; P Campbell
Journal:  J Pediatr       Date:  1975-03       Impact factor: 4.406

2.  Axonal filamentous spheroids associated with cardiomyopathy with "targetoid fibers". I. Clinical, histologic, and electron microscopic studies.

Authors:  H M Liu; M Gumbinas
Journal:  Neurology       Date:  1974-06       Impact factor: 9.910

3.  [Disorders of neuronal migration in Zellwegers cerebrohepato-renal syndrome (author's transl)].

Authors:  F Garzuly; L Szabo; L Kadas
Journal:  Neuropadiatrie       Date:  1974-08

4.  An analysis of the ultrastructural findings in infantile neuroaxonal dystrophy (Seitelberger's disease).

Authors:  H M Liu; M Larson; Y Mizuno
Journal:  Acta Neuropathol       Date:  1974-03-26       Impact factor: 17.088

5.  Cerebro-hepato-renal syndrome of Zellweger: an inherited disorder of neuronal migration.

Authors:  J J Volpe; R D Adams
Journal:  Acta Neuropathol       Date:  1972       Impact factor: 17.088

6.  Congenital and familial iron overload.

Authors:  L Vitale; J M Opitz; N T Shahidi
Journal:  N Engl J Med       Date:  1969-03-20       Impact factor: 91.245

7.  Neurofibrillary pathology.

Authors:  H Wiśniewski; R D Terry; A Hirano
Journal:  J Neuropathol Exp Neurol       Date:  1970-04       Impact factor: 3.685

8.  A syndrome of multiple developmental defects including polycystic kidneys and intrahepatic biliary dysgenesis in 2 siblings.

Authors:  D W Smith; J M Opitz; S L Inhorn
Journal:  J Pediatr       Date:  1965-10       Impact factor: 4.406

9.  Neuroaxonal dystrophy in congenital biliary atresia.

Authors:  J H Sung; E M Stadlan
Journal:  J Neuropathol Exp Neurol       Date:  1966-07       Impact factor: 3.685

10.  Inhibition of protein synthesis in Krebs 2 ascites cells and cell-free systems by phenylalanine and its effect on leucine and lysine in the amino acid pool.

Authors:  J P Roscoe; M D Eaton; G C Choy
Journal:  Biochem J       Date:  1968-10       Impact factor: 3.857

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  9 in total

Review 1.  Genetics of the polymicrogyria syndromes.

Authors:  A Jansen; E Andermann
Journal:  J Med Genet       Date:  2005-05       Impact factor: 6.318

2.  A pathological study of a peripheral nerve in a case of neonatal adrenoleukodystrophy.

Authors:  T Mito; K Takada; S Akaboshi; S Takashima; K Takeshita; Y Origuchi
Journal:  Acta Neuropathol       Date:  1989       Impact factor: 17.088

3.  The Zellweger syndrome: subcellular pathology, neuropathology, and the demonstration of pneumocystis carinii pneumonitis in two siblings.

Authors:  A Brun; M Gilboa; G W Meeuwisse; H Nordgren
Journal:  Eur J Pediatr       Date:  1978-04-20       Impact factor: 3.183

4.  Subependymal germinolytic cysts in Zellweger syndrome.

Authors:  I M Russel; L van Sonderen; H L van Straaten; P G Barth
Journal:  Pediatr Radiol       Date:  1995

5.  The mechanism of arrest of neuronal migration in the Zellweger malformation: an hypothesis bases upon cytoarchitectonic analysis.

Authors:  P Evrard; V S Caviness; J Prats-Vinas; G Lyon
Journal:  Acta Neuropathol       Date:  1978-02-20       Impact factor: 17.088

6.  Peroxisomal beta-oxidation defect with detectable peroxisomes: a case with neonatal onset and progressive course.

Authors:  P G Barth; R J Wanders; R B Schutgens; E M Bleeker-Wagemakers; D van Heemstra
Journal:  Eur J Pediatr       Date:  1990-07       Impact factor: 3.183

7.  [Morphology and diagnosis of Zellweger syndrome. A contribution to combined cytochemical-finestructural identification of peroxisomes in autopsy material and frozen liver tissue with case report].

Authors:  J Müller-Höcker; K Bise; W Endres; G Hübner
Journal:  Virchows Arch A Pathol Anat Histol       Date:  1981

8.  A Golgi study of the brain malformation in Zellweger's cerebro-hepato-renal disease.

Authors:  E Della Giustina; A M Goffinet; P Landrieu; G Lyon
Journal:  Acta Neuropathol       Date:  1981       Impact factor: 17.088

9.  TMX2 Is a Crucial Regulator of Cellular Redox State, and Its Dysfunction Causes Severe Brain Developmental Abnormalities.

Authors:  Laura V Vandervore; Rachel Schot; Chiara Milanese; Daphne J Smits; Esmee Kasteleijn; Andrew E Fry; Daniela T Pilz; Stefanie Brock; Esra Börklü-Yücel; Marco Post; Nadia Bahi-Buisson; María José Sánchez-Soler; Marjon van Slegtenhorst; Boris Keren; Alexandra Afenjar; Stephanie A Coury; Wen-Hann Tan; Renske Oegema; Linda S de Vries; Katherine A Fawcett; Peter G J Nikkels; Aida Bertoli-Avella; Amal Al Hashem; Abdulmalik A Alwabel; Kalthoum Tlili-Graiess; Stephanie Efthymiou; Faisal Zafar; Nuzhat Rana; Farah Bibi; Henry Houlden; Reza Maroofian; Richard E Person; Amy Crunk; Juliann M Savatt; Lisbeth Turner; Mohammad Doosti; Ehsan Ghayoor Karimiani; Nebal Waill Saadi; Javad Akhondian; Maarten H Lequin; Hülya Kayserili; Peter J van der Spek; Anna C Jansen; Johan M Kros; Robert M Verdijk; Nataša Jovanov Milošević; Maarten Fornerod; Pier Giorgio Mastroberardino; Grazia M S Mancini
Journal:  Am J Hum Genet       Date:  2019-11-14       Impact factor: 11.025

  9 in total

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