Literature DB >> 2918537

Hereditary distal muscular atrophy with vocal cord paralysis and sensorineural hearing loss: a dominant form of spinal muscular atrophy?

E Boltshauser1, W Lang, T Spillmann, E Hof.   

Abstract

In 1980 Young and Harper described a family with an unusual form of distal spinal muscular atrophy associated with vocal cord paralysis. We report a family with three similarly affected subjects. Progressive sensorineural hearing loss was an additional feature in our patients. Electrophysiological and histological investigations did not exclude an involvement of sensory neurones. Whether the classification of this dominant disorder with the spinal muscular atrophies is justified will depend on additional studies in further families.

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Year:  1989        PMID: 2918537      PMCID: PMC1015559          DOI: 10.1136/jmg.26.2.105

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  12 in total

1.  CONGENITAL LARYNGEAL-ABDUCTOR PARALYSIS DUE TO NUCLEUS AMBIGUUS DYSGENESIS IN THREE BROTHERS.

Authors:  D PLOTT
Journal:  N Engl J Med       Date:  1964-09-17       Impact factor: 91.245

2.  Familial laryngeal abductor paralysis and psychomotor retardation.

Authors:  G V Watters; N Fitch
Journal:  Clin Genet       Date:  1973       Impact factor: 4.438

3.  The normal sural nerve in man. I. Ultrastructure and numbers of fibres and cells.

Authors:  J Ochoa; W G Mair
Journal:  Acta Neuropathol       Date:  1969       Impact factor: 17.088

4.  Distal spinal muscular atrophy. A clinical and genetic study of 8 kindreds.

Authors:  J Pearn; P Hudgson
Journal:  J Neurol Sci       Date:  1979-10       Impact factor: 3.181

5.  Facioscapulohumeral dystrophy associated with hearing loss and Coats syndrome.

Authors:  D A Taylor; J E Carroll; M E Smith; M O Johnson; G P Johnston; M H Brooke
Journal:  Ann Neurol       Date:  1982-10       Impact factor: 10.422

6.  Familial vocal cord dysfunction.

Authors:  M J Cunningham; R D Eavey; D C Shannon
Journal:  Pediatrics       Date:  1985-11       Impact factor: 7.124

7.  Late-onset X-linked recessive spinal and bulbar muscular atrophy.

Authors:  S P Ringel; N S Lava; M M Treihaft; M L Lubs; H A Lubs
Journal:  Muscle Nerve       Date:  1978 Jul-Aug       Impact factor: 3.217

8.  Hereditary distal spinal muscular atrophy. A report on 34 cases and a review of the literature.

Authors:  A E Harding; P K Thomas
Journal:  J Neurol Sci       Date:  1980-03       Impact factor: 3.181

9.  [Chronic spinal amyotrophy with paralysis of the vocal cords: Young-Harper syndrome].

Authors:  G Serratrice; J F Pellissier; J L Gastaut; C Desnuelle
Journal:  Rev Neurol (Paris)       Date:  1984       Impact factor: 2.607

10.  Hereditary distal spinal muscular atrophy with vocal cord paralysis.

Authors:  I D Young; P S Harper
Journal:  J Neurol Neurosurg Psychiatry       Date:  1980-05       Impact factor: 10.154

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  7 in total

1.  Localization of the gene for distal hereditary motor neuronopathy VII (dHMN-VII) to chromosome 2q14.

Authors:  M McEntagart; N Norton; H Williams; M D Teare; M Dunstan; P Baker; H Houlden; M Reilly; N Wood; P S Harper; P A Futreal; N Williams; N Rahman
Journal:  Am J Hum Genet       Date:  2001-04-04       Impact factor: 11.025

2.  A unique point mutation in the PMP22 gene is associated with Charcot-Marie-Tooth disease and deafness.

Authors:  M J Kovach; J P Lin; S Boyadjiev; K Campbell; L Mazzeo; K Herman; L A Rimer; W Frank; B Llewellyn; E W Jabs; D Gelber; V E Kimonis
Journal:  Am J Hum Genet       Date:  1999-06       Impact factor: 11.025

3.  Dominant mutations in the cation channel gene transient receptor potential vanilloid 4 cause an unusual spectrum of neuropathies.

Authors:  Magdalena Zimoń; Jonathan Baets; Michaela Auer-Grumbach; José Berciano; Antonio Garcia; Eduardo Lopez-Laso; Luciano Merlini; David Hilton-Jones; Meriel McEntagart; Andrew H Crosby; Nina Barisic; Eugen Boltshauser; Christopher E Shaw; Guida Landouré; Christy L Ludlow; Rachelle Gaudet; Henry Houlden; Mary M Reilly; Kenneth H Fischbeck; Charlotte J Sumner; Vincent Timmerman; Albena Jordanova; Peter De Jonghe
Journal:  Brain       Date:  2010-05-11       Impact factor: 13.501

4.  Reduced penetrance in hereditary motor neuropathy caused by TRPV4 Arg269Cys mutation.

Authors:  José Berciano; Jonathan Baets; Elena Gallardo; Magdalena Zimoń; Antonio García; Eduardo López-Laso; Onofre Combarros; Jon Infante; Vincent Timmerman; Albena Jordanova; Peter De Jonghe
Journal:  J Neurol       Date:  2011-02-19       Impact factor: 4.849

Review 5.  Brown-Vialetto-Van Laere syndrome.

Authors:  Sivakumar Sathasivam
Journal:  Orphanet J Rare Dis       Date:  2008-04-17       Impact factor: 4.123

6.  Pontobulbar palsy and sensorineural deafness (Brown-Vialetto-van Laere syndrome): A case from Northwest Iran.

Authors:  Vahideh Toopchizadeh; Masood Ghahvechi Akbari; Afshin Habibzadeh
Journal:  J Pediatr Neurosci       Date:  2013-09

7.  Madras motor neuron disease (MMND) is distinct from the riboflavin transporter genetic defects that cause Brown-Vialetto-Van Laere syndrome.

Authors:  Atchayaram Nalini; Amelie Pandraud; Kin Mok; Henry Houlden
Journal:  J Neurol Sci       Date:  2013-08-13       Impact factor: 3.181

  7 in total

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