Literature DB >> 9217208

Earliest evidence for arthrogryposis multiplex congenita or Larsen syndrome?

T Anderson1.   

Abstract

A sixteenth-century illustrated pamphlet from Great Britain suggests that documentary evidence may permit accurate diagnosis of pathological conditions in earlier societies. The document is of particular importance, since the presented congenital abnormalities, including cleft lip, spina bifida cystica, genu recurvatum, and talipes deformity are reported rarely in archaeological skeletal material. It is suggested that the combination of abnormalities may represent the earliest case of arthrogryposis multiplex congenita or Larsen syndrome.

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Year:  1997        PMID: 9217208

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


  2 in total

1.  Arthrogryposis multiplex congenita (AMC), a hereditary disease in swine, maps to chromosome 5 by linkage analysis.

Authors:  Sem Genini; Massoud Malek; Spela Spilar; Trung Thanh Nguyen; Frédéric Ménétrey; Stefen Gebert; Christian Hagger; Stefan Neuenschwander; Haja N Kadarmideen; Gerald Stranzinger; Peter Vögeli
Journal:  Mamm Genome       Date:  2004-11       Impact factor: 2.957

2.  The diagnosis of art: arthrogryposis and Ribera's The Clubfoot.

Authors:  Manoj Ramachandran; Jeffrey K Aronson
Journal:  J R Soc Med       Date:  2006-06       Impact factor: 18.000

  2 in total

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