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Xu, C. Langer Mesomelic Dysplasia. Encyclopedia. Available online: https://encyclopedia.pub/entry/4481 (accessed on 28 September 2026).
Xu C. Langer Mesomelic Dysplasia. Encyclopedia. Available at: https://encyclopedia.pub/entry/4481. Accessed September 28, 2026.
Xu, Camila. "Langer Mesomelic Dysplasia" Encyclopedia, https://encyclopedia.pub/entry/4481 (accessed September 28, 2026).
Xu, C. (2020, December 23). Langer Mesomelic Dysplasia. In Encyclopedia. https://encyclopedia.pub/entry/4481
Xu, Camila. "Langer Mesomelic Dysplasia." Encyclopedia. Web. 23 December, 2020.
Langer Mesomelic Dysplasia
Edit

Langer mesomelic dysplasia is a disorder of bone growth.

genetic conditions

References

  1. Bertorelli R, Capone L, Ambrosetti F, Garavelli L, Varriale L, Mazza V,Stanghellini I, Percesepe A, Forabosco A. The homozygous deletion of the 3'enhancer of the SHOX gene causes Langer mesomelic dysplasia. Clin Genet. 2007Nov;72(5):490-1.
  2. Campos-Barros A, Benito-Sanz S, Ross JL, Zinn AR, Heath KE. Compoundheterozygosity of SHOX-encompassing and downstream PAR1 deletions results inLanger mesomelic dysplasia (LMD). Am J Med Genet A. 2007 May 1;143A(9):933-8.
  3. Shears DJ, Guillen-Navarro E, Sempere-Miralles M, Domingo-Jimenez R, Scambler PJ, Winter RM. Pseudodominant inheritance of Langer mesomelic dysplasia caused bya SHOX homeobox missense mutation. Am J Med Genet. 2002 Jun 15;110(2):153-7.
  4. Thomas NS, Maloney V, Bass P, Mulik V, Wellesley D, Castle B. SHOX mutationsin a family and a fetus with Langer mesomelic dwarfism. Am J Med Genet A. 2004Jul 15;128A(2):179-84.
  5. Zinn AR, Wei F, Zhang L, Elder FF, Scott CI Jr, Marttila P, Ross JL. Complete SHOX deficiency causes Langer mesomelic dysplasia. Am J Med Genet. 2002 Jun15;110(2):158-63.
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Update Date: 23 Dec 2020
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