Literature DB >> 6200796

The Wiedemann-Rautenstrauch or neonatal progeroid syndrome. Neuropathological study of a case.

J J Martin, C M Ceuterick, J G Leroy, E A Devos, J G Roelens.   

Abstract

Neuropathological data from the autopsy of a 5 1/2 year-old female patient with the Wiedemann-Rautenstrauch or neonatal progeroid syndrome are reported. Extensive demyelination is found in the central nervous system with occasionally a tigroid pattern and with large amounts of neutral fats and intermediate debris of myelin breakdown in macrophages. These lesions are characteristic of pure sudanophilic leucodystrophy. Features differentiating the findings from those in Pelizaeus-Merzbacher disease and in other disorders associated with sudanophilic leucodystrophy with various special characteristics are presented and discussed.

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Year:  1984        PMID: 6200796     DOI: 10.1055/s-2008-1052339

Source DB:  PubMed          Journal:  Neuropediatrics        ISSN: 0174-304X            Impact factor:   1.947


  7 in total

1.  Wiedemann-Rautenstrauch syndrome: first Indian case.

Authors:  Meenu Pandey; Neeraja Gupta; Madhulika Kabra; Ajay Kumar; Vikram Datta; Arvind Saili
Journal:  Indian J Pediatr       Date:  2011-06-01       Impact factor: 1.967

2.  A maternally transmitted lethal neonatal progeroid syndrome with prominent genitourinary and gastrointestinal features.

Authors:  M B Delatycki; M A Cleary; A Bankier; P N McDougall; J S Ahluwalia; C W Chow; C M Cooke-Yarborough
Journal:  J Med Genet       Date:  1997-06       Impact factor: 6.318

3.  Wiedemann-Rautenstrauch syndrome.

Authors:  H V Toriello
Journal:  J Med Genet       Date:  1990-04       Impact factor: 6.318

4.  Wiedemann-Rautenstrauch neonatal progeroid syndrome: report of three new patients.

Authors:  H Arboleda; L Quintero; E Yunis
Journal:  J Med Genet       Date:  1997-05       Impact factor: 6.318

Review 5.  Two sibs with Wiedemann-Rautenstrauch syndrome: possibilities of prenatal diagnosis by ultrasound.

Authors:  G Castiñeyra; M Panal; H Lopez Presas; E Goldschmidt; J M Sánchez
Journal:  J Med Genet       Date:  1992-06       Impact factor: 6.318

6.  LMNA is mutated in Hutchinson-Gilford progeria (MIM 176670) but not in Wiedemann-Rautenstrauch progeroid syndrome (MIM 264090).

Authors:  Henian Cao; Robert A Hegele
Journal:  J Hum Genet       Date:  2003-04-03       Impact factor: 3.172

Review 7.  The neonatal pseudo-hydrocephalic progeroid syndrome (Wiedemann-Rautenstrauch). Report of a new patient and review of the literature.

Authors:  C Rudin; L Thommen; C Fliegel; B Steinmann; U Bühler
Journal:  Eur J Pediatr       Date:  1988-05       Impact factor: 3.183

  7 in total

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