Literature DB >> 6862838

Progressive bulbar paralysis in childhood: a case report.

G F Perticoni, T A Cantisani, H Fisher.   

Abstract

The case of a progressive bulbar paresis in a nine and a half year old child is reported. The first symptoms were present at birth; however, the subsequent evolution was very low. Lesion of the motor nuclei of the V, VII, IX, XII, cranial nerves was evident on electromyographic investigation. Damage to the acoustic brain stem pathway was documented by the brain stem evoked potentials although audiometry was normal. No other neuronal systems or districts appeared to be damaged. The case suggests Fazio-Londe disease, although the involvement (albeit partial) of the auditory pathways recalls Van Laere syndrome. This supports the view that motor neuron disease in infancy is not an autonomous entity but a variant in a wide spectrum of progressive neuronal diseases.

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Year:  1983        PMID: 6862838     DOI: 10.1007/bf02043448

Source DB:  PubMed          Journal:  Ital J Neurol Sci        ISSN: 0392-0461


  14 in total

1.  Infantile muscular atrophy.

Authors:  R K BYERS; B Q BANKER
Journal:  Arch Neurol       Date:  1961-08

2.  Progressive bulbar paralysis in childhood (Fazio-Londe's disease). Report of a case with pathologic evidence of nuclear atrophy.

Authors:  M R GOMEZ; V CLERMONT; J BERNSTEIN
Journal:  Arch Neurol       Date:  1962-04

3.  [Forty cases of Werdnig-Hoffmann disease with eleven anatomical examinations].

Authors:  S THIEFFRY; M ARTHUIS; E BARGETON
Journal:  Rev Neurol (Paris)       Date:  1955-10       Impact factor: 2.607

4.  The central nervous system in motor neurone disease.

Authors:  B Brownell; D R Oppenheimer; J T Hughes
Journal:  J Neurol Neurosurg Psychiatry       Date:  1970-06       Impact factor: 10.154

5.  [Chronic progressive bulbo-pontine paralysis with deafness: a case of Fio-Londe syndrome].

Authors:  G Arnould; P Tridon; M Laxenaire; L Picard; M Weber; B Brichet
Journal:  Rev Otoneuroophtalmol       Date:  1968-04

6.  Progressive bulbar paralysis in childhood (Londe syndrome). A clinicopathological report.

Authors:  E Della Giustina; G Ferrière; P Evrard; G Lyon
Journal:  Acta Paediatr Belg       Date:  1979 Apr-Jun

7.  [Familial progressive chronic bulbo-pontine paralysis with deafness. A case of Klippel-Trenaunay syndrome in siblings of the same family. Diagnostic and genetic problems].

Authors:  J Van Laere
Journal:  Rev Neurol (Paris)       Date:  1966-08       Impact factor: 2.607

8.  Progressive bulbar paresis in childhood.

Authors:  M P Alexander; E S Emery; F C Koerner
Journal:  Arch Neurol       Date:  1976-01

9.  Progressive bulbar paralysis associated with neural deafness. A nosological entity.

Authors:  R Alberca; C Montero; A Ibañez; D I Segura; G Miranda-Nieves
Journal:  Arch Neurol       Date:  1980-04

10.  [Dilator paralysis of the glottis in lateral amyotrophic sclerosis].

Authors:  T ALAJOUANINE; M BOUCHET; P PIALOUX; F LHERMITTE
Journal:  Rev Neurol (Paris)       Date:  1953       Impact factor: 2.607

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  2 in total

1.  Progressive bulbur paralysis (Fazio-Londe disease).

Authors:  Taruna Gulati; Vivek Dewan; Praveen Kumar; Bina Ahuja; V K Anand
Journal:  Indian J Pediatr       Date:  2004-01       Impact factor: 1.967

Review 2.  The Brown-Vialetto-Van Laere and Fazio Londe syndrome revisited: natural history, genetics, treatment and future perspectives.

Authors:  Annet M Bosch; Kevin Stroek; Nico G Abeling; Hans R Waterham; Lodewijk Ijlst; Ronald J A Wanders
Journal:  Orphanet J Rare Dis       Date:  2012-10-29       Impact factor: 4.123

  2 in total

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