Literature DB >> 2732993

Moore-Federman syndrome and acromicric dysplasia: are they the same entity?

R M Winter1, M A Patton, J Challener, R F Mueller, M Baraitser.   

Abstract

Four unrelated patients are reported with short stature, stiffness of the joints, short fingers, inability to make a fist, and thickened skin on the forearms. Investigations have failed to show a lysosomal storage disorder and radiographs show non-specific changes with a delayed carpal bone age. The clinical features in the four children are very similar to the recently described acromicric dysplasia. There are also similarities to Moore-Federman syndrome which has only been described in one family. The case is made that acromicric dysplasia and Moore-Federman syndrome are the same entity.

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Year:  1989        PMID: 2732993      PMCID: PMC1015599          DOI: 10.1136/jmg.26.5.320

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


  5 in total

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Journal:  Arch Intern Med       Date:  1965-04

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Journal:  J Pediatr       Date:  1977-12       Impact factor: 4.406

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Journal:  Am J Med Genet       Date:  1984-11

5.  Acromicric dysplasia.

Authors:  P Maroteaux; R Stanescu; V Stanescu; R Rappaport
Journal:  Am J Med Genet       Date:  1986-07
  5 in total
  4 in total

1.  Spherophakia, nanophthalmia, hypoplastic ciliary body and glaucoma in brachydactyly-associated syndromes.

Authors:  T S Dietlein; H Mietz; P C Jacobi; G K Krieglstein
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  1996-08       Impact factor: 3.117

2.  Acromicric dysplasia and geleophysic dysplasia: similarities and differences.

Authors:  R C Hennekam; Y van Bever; J W Oorthuys
Journal:  Eur J Pediatr       Date:  1996-04       Impact factor: 3.183

3.  Reviving the Moore-Federman syndrome.

Authors:  J M Fell; R Stanhope
Journal:  J R Soc Med       Date:  1993-01       Impact factor: 5.344

4.  Acromicric dysplasia: long term outcome and evidence of autosomal dominant inheritance.

Authors:  L Faivre; M Le Merrer; C Baumann; M Polak; P Chatelain; V Sulmont; J Cousin; M Bost; M P Cordier; E Zackai; K Russell; G Finidori; J C Pouliquen; A Munnich; P Maroteaux; V Cormier-Daire
Journal:  J Med Genet       Date:  2001-11       Impact factor: 6.318

  4 in total

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