Literature DB >> 568685

[Spongious cerebral dystrophy at an infant age (Canavan-Bogaert-Bertrand types) in three siblings of a non-Jewish family in upper Franconia (author's transl)].

H Schmidt, H D Rott, G Neuhäuser, W Neumann.   

Abstract

A daughter and two sons of possibly consangineous parents died after motor and mental deterioration at 18, 16 and 15 months of age. Spongy degeneration of the CNS (Canavan-van-Bogaert-Bertrand type) was diagnosed on neuropathological examinationtion; the histological findings were almost identical in the patients. Own clinical experiences are compared with reports from the literature; data important in clinical and differential diagnosis are reviewed. Pathogenetical and etiological aspects are discussed; autosomal recessive inheritance has to be considered in genetic counselling.

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Year:  1978        PMID: 568685

Source DB:  PubMed          Journal:  Klin Padiatr        ISSN: 0300-8630            Impact factor:   1.349


  2 in total

1.  Protracted form of Canavan's disease: case history and protein kinase activity of membrane fractions.

Authors:  D H Boehme; N Marks
Journal:  Acta Neuropathol       Date:  1981       Impact factor: 17.088

2.  The Clinical Features and Diagnosis of Canavan's Disease: A Case Series of Iranian Patients.

Authors:  Parvaneh Karimzadeh; Narjes Jafari; Habibe Nejad Biglari; Elham Rahimian; Farzad Ahmadabadi; Hamid Nemati; Mohamad Mehdi Nasehi; Mohammad Ghofrani; Mohsen Mollamohammadi
Journal:  Iran J Child Neurol       Date:  2014
  2 in total

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