Literature DB >> 8387243

Sandrow syndrome of mirror hands and feet and facial abnormalities.

N Kogekar1, A S Teebi, J Vockley.   

Abstract

In 1970, Sandrow et al. (J Bone Joint Surg 52-A:363-370) described a syndrome of ulnar and fibular dimelia with facial abnormalities present in 2 generations in a family. We describe a new patient with similar manifestations, establishing this constellation of anomalies as a distinct syndrome.

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Year:  1993        PMID： 8387243     DOI： 10.1002/ajmg.1320460204

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN： 0148-7299


  5 in total

1.  Mirror foot: treatment of three cases and review of the literature.

Authors:  Hodaka Fukazawa; Hidehiko Kawabata; Yoshito Matsui
Journal:  J Child Orthop       Date:  2009-07-07       Impact factor: 1.548

2.  Mirror hands and feet: a further case of Laurin-Sandrow syndrome.

Authors:  E Hatchwell; N Dennis
Journal:  J Med Genet       Date:  1996-05       Impact factor: 6.318

3.  Mirror hands and feet.

Authors:  M A van Steensel
Journal:  J Med Genet       Date:  1997-08       Impact factor: 6.318

Review 4.  Laurin-Sandrow syndrome (mirror hands and feet and nasal defects): description of a new case.

Authors:  M L Martínez-Frías; M Alcaraz; P Espejo; M A Gómez; R García de León; L González Moro
Journal:  J Med Genet       Date:  1994-05       Impact factor: 6.318

5.  Pre-axial mirror polydactyly associated with tibial deficiency: a study of the patterns of skeletal anomalies of the foot and leg.

Authors:  Renjit Verghese; Hitesh Shah; Gleeson Rebello; Benjamin Joseph
Journal:  J Child Orthop       Date:  2007-02-03       Impact factor: 1.548
  5 in total

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