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Chondrodysplasia Blomstrand
Other namesBlomstrand's lethal chondrodysplasia
This condition is inherited in an autosomal recessive manner.

Chondrodysplasia Blomstrand is a rare genetic disorder characterized by a mutation of the parathyroid hormone receptor, leading to the absence of a functional PTHR1. This condition causes abnormal ossification of the endocrine system and intermembranous tissues,[1] along with accelerated skeletal maturation.[2]

References[edit]

  1. ^ Bilezikian, John P.; Raisz, Lawrence G.; Martin, T. John Martin (2008). Principles of Bone Biology. Academic Press. p. 610. ISBN 9780123738844.
  2. ^ Glorieux, Francis H.; Pettifor, John M.; Jüppner, Harald (2011). Pediatric Bone: Biology & Diseases. Academic Press. p. 46. ISBN 9780123820402.

External links[edit]


source: https://en.wikipedia.org/wiki/Chondrodysplasia_Blomstrand

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