Literature DB >> 1568849

The Wolfram syndrome: a primary neurodegenerative disorder with lethal potential.

B T Kinsley1, R G Firth.   

Abstract

We describe four cases of the Wolfram syndrome; a rare congenital syndrome characterised in it's complete form by diabetes mellitus, diabetes insipidus, optic atrophy, nerve deafness and dilatation of the urinary tract. All four of the cases described developed grand mal epilepsy in their second and third decades. Two of the cases developed progressive ataxia. There was one death due to status epilepticus. Absence of most of the corpus callosum and of the septum pellucidum was noted at autopsy. This pathological finding has not been reported previously in this syndrome. These cases highlight the neuro-degenerative aspects of the Wolfram syndrome. The literature on neurological aspects of the syndrome is reviewed.

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Year:  1992        PMID: 1568849

Source DB:  PubMed          Journal:  Ir Med J        ISSN: 0332-3102


  1 in total

Review 1.  Mitochondrial mutation commonly associated with Leber's hereditary optic neuropathy observed in a patient with Wolfram syndrome (DIDMOAD).

Authors:  D Pilz; O W Quarrell; E W Jones
Journal:  J Med Genet       Date:  1994-04       Impact factor: 6.318

  1 in total

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