Literature DB >> 6716408

Late infantile autosomal recessive myotonia, mental retardation, and skeletal abnormalities: a new autosomal recessive syndrome.

A Richieri-Costa, S M Garcia da Silva, O Frota-Pessoa.   

Abstract

Four sibs of non-consanguineous parents who had myotonia from late infancy are described. Mild to moderate mental retardation, severe bone abnormalities of the vertebral column (mainly in the thoracolumbar region), and short stature were also observed. Autosomal recessive inheritance is demonstrated. These cases are compared with reported cases of the Schwartz-Jampel syndrome.

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Mesh:

Year:  1984        PMID: 6716408      PMCID: PMC1049235          DOI: 10.1136/jmg.21.2.103

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


  9 in total

1.  Congenital blepharophimosis associated with a unique generalized myopathy.

Authors:  O SCHWARTZ; R S JAMPEL
Journal:  Arch Ophthalmol       Date:  1962-07

2.  Chondrodystrophic myotonia. A report of two unrelated Dutch patients.

Authors:  A C van Huffelen; F J Gabreĕls; J S Luypen-vd Horst; J L Slooff; A M Stadhouders; J J Korten
Journal:  Neuropadiatrie       Date:  1974-02

3.  The Schwartz-Jampel syndrome. Its clinical, physiological and histological expressions.

Authors:  W M Fowler; R B Layzer; R G Taylor; E D Eberle; G E Sims; T L Munsat; M Philippart; B W Wilson
Journal:  J Neurol Sci       Date:  1974-05       Impact factor: 3.181

4.  The schwartz syndrome in southern africa.

Authors:  P Beighton
Journal:  Clin Genet       Date:  1973-06       Impact factor: 4.438

5.  Schwartz syndrome: myotonia with blepharophimosis and limitation of joints.

Authors:  M Saadat; H Mokfi; H Vakil; M Ziai
Journal:  J Pediatr       Date:  1972-08       Impact factor: 4.406

6.  Myotonia, dwarfism, diffuse bone disease and unusual ocular and facial abnormalities (a new syndrome).

Authors:  D C Aberfeld; L P Hinterbuchner; M Schneider
Journal:  Brain       Date:  1965-06       Impact factor: 13.501

7.  Osteo-chondro-muscular dystrophy. A disorder manifested by multiple skeletal deformities, myotonia, and dystrophic changes in muscle.

Authors:  P R Huttenlocher; J Landwirth; V Hanson; B B Gallagher; K Bensch
Journal:  Pediatrics       Date:  1969-12       Impact factor: 7.124

8.  Chondrodystrophic myotonia: report of two cases. Myotonia, dwarfism, diffuse bone disease, and unusual ocular and facial abnormalities.

Authors:  D C Aberfeld; T Namba; M V Vye; D Grob
Journal:  Arch Neurol       Date:  1970-05

9.  Myotonia, shortness of stature, and hip dysplasia. Schwartz-Jampel syndrome.

Authors:  T R Mereu; I H Porter; G Hug
Journal:  Am J Dis Child       Date:  1969-04
  9 in total

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