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Last Updated: Oct 11, 2012 - 10:22:56 PM
Brachydactyly Channel

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Latest Research : Genetics : Genetic Disorders : Brachydactyly

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Putting a finger on shortened digits

Apr 3, 2005 - 1:44:00 PM
The mice have disrupted Shh expression – a factor that helps skeletal formation. The result is that the mice have symptoms similar to human brachydactyly type A1. This is because the misexpression of Shh disrupts other factors with normally regulate joint development as well as the growth and patterning of the digits

 
[RxPG] Brachydactyly is a group of inherited disorders of the hands that are characterized by shortened fingers and abnormal joint formation.

In a paper appearing in the April 1 issue of The Journal of Clinical Investigation, Stefan Mundlos and colleagues from the Max Planck Institute for Molecular Genetics describe the analysis of a mouse model with limb mutations called short digits (Dsh).

The mice have disrupted Shh expression – a factor that helps skeletal formation. The result is that the mice have symptoms similar to human brachydactyly type A1. This is because the misexpression of Shh disrupts other factors with normally regulate joint development as well as the growth and patterning of the digits

Luis de la Fuente and Jill Helms write, in an accompanying commentary, that this study shows "that removal or expansion of one of the factors that contributes to the establishment of a boundary can cause a multitude of processes, including those that shape and control development of the skeleton, then go awry." The developmental pathology associated with Shh misexpression extends our understanding of the developmental pathology of digit development and thus of human brachydactyly.



Publication: TITLE: An inversion involving the mouse Shh locus results in brachydactyly through dysregulation of Shh expression
On the web: View the PDF of this article 

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 Additional information about the news article
TITLE: An inversion involving the mouse Shh locus results in brachydactyly through dysregulation of Shh expression

AUTHOR CONTACT:
Stefan Mundlos
Max Planck Institute for Molecular Genetics, Berlin, Germany.
Phone: +49-30-8413-1267; Fax: +49-30-8413-1385; E-mail: [email protected]

View the PDF of this article at: https://www.the-jci.org/article.php?id=23675

ACCOMPANYING COMMENTARY:

TITLE: The fickle finger of fate

AUTHOR CONTACT:
Jill A. Helms
Stanford University, Stanford, California, USA.
Phone: (650) 736-0919; Fax: (650) 736-4374; E-mail: [email protected]
View the PDF of this article at: https://www.the-jci.org/article.php?id=24840
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