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Acromesomelic dysplasia

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This is an old revision of this page, as edited by Cydebot (talk | contribs) at 16:38, 20 September 2016 (Robot - Moving category Genetic disorders to Category:Genetic diseases and disorders per CFD at Wikipedia:Categories for discussion/Log/2016 September 12.). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

Acromesomelic dysplasia is a rare skeletal disorder that causes abnormal bone and cartilage development, leading to shortening of the forearms, lower legs, hands, feet, fingers, and toes. Five different genetic mutations have been implicated. Treatment is individualized but is generally aimed at palliating symptoms, for example, treatment of kyphosis and lumbar hyperlordosis.[1]

References

Template:Research help

  1. ^ "Acromesomelic Dysplasia - NORD (National Organization for Rare Disorders)". Retrieved 2015-09-19.