Literature DB >> 739527

The Marden-Walker syndrome.

C R King, E Magenis.   

Abstract

The characteristic facies, joint contractures, muscular hypotonia, and growth and developmental delay of the Marden-Walker syndrome were present in a 19-month-old boy. Extensive evaluation of the neuromuscular system failed to identify a specific abnormality. Electromyography was normal with low amplitude. Light and electron microscopy of a skeletal muscle biopsy was normal. Histochemical study of this biopsy material was also normal. The pathogenesis of the syndrome is discussed.

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Mesh:

Year:  1978        PMID: 739527      PMCID: PMC1013733          DOI: 10.1136/jmg.15.5.366

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


  10 in total

1.  [2 CASES OF CRANIO-FACIAL MALFORMATIONS. 1. MICROPHTHALMIA ("OCULO-PALPEBRAL NANISM") WITH CRANIO-FACIAL DYSOSTOSIS AND DYSRRHAPHIA; 2. MANDIBULOOCULO-FACIAL DYSMORPHISM (HALLERMANN-STREIFF SYNDROME)].

Authors:  S YOUNESSIAN; F AMMANN
Journal:  Ophthalmologica       Date:  1964       Impact factor: 3.250

2.  Congenital blepharophimosis associated with a unique generalized myopathy.

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

3.  Older paternal age and fresh gene mutation: data on additional disorders.

Authors:  K L Jones; D W Smith; M A Harvey; B D Hall; L Quan
Journal:  J Pediatr       Date:  1975-01       Impact factor: 4.406

4.  Marden-Walker syndrome.

Authors:  E Passarge
Journal:  Birth Defects Orig Artic Ser       Date:  1975

5.  Probable Marden-Walker syndrome: evidence for autosomal recessive inheritance.

Authors:  S A Temtamy; A S Shoukry; M Raafat; S Mihareb
Journal:  Birth Defects Orig Artic Ser       Date:  1975

6.  A child with facial and skeletal dysmorphia reminiscent of Schwartz syndrome.

Authors:  J L Simpson; M Degnan
Journal:  Birth Defects Orig Artic Ser       Date:  1975

7.  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

8.  Congenital blepharophimosis, joint contractures, and muscular hypotonia.

Authors:  N Fitch; G Karpati; L Pinsky
Journal:  Neurology       Date:  1971-12       Impact factor: 9.910

9.  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

10.  A new generalized connective tissue syndrome.

Authors:  P M Marden; W A Walker
Journal:  Am J Dis Child       Date:  1966-09
  10 in total
  4 in total

1.  Linkage analysis in blepharophimosis-ptosis syndrome confirms localisation to 3q21-24.

Authors:  H S Harrar; S Jeffery; M A Patton
Journal:  J Med Genet       Date:  1995-10       Impact factor: 6.318

2.  Two brothers with the Marden-Walker syndrome: case report and review.

Authors:  F M Howard; P Rowlandson
Journal:  J Med Genet       Date:  1981-02       Impact factor: 6.318

3.  A 26-month-old child with Marden-Walker syndrome and pyloric stenosis.

Authors:  D Gossage; J M Perrin; M G Butler
Journal:  Am J Med Genet       Date:  1987-04

4.  Blepharophimosis, ptosis, epicanthus inversus syndrome (BPES syndrome)

Authors:  C Oley; M Baraitser
Journal:  J Med Genet       Date:  1988-01       Impact factor: 6.318

  4 in total

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