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Xu, C. Hypochondrogenesis. Encyclopedia. Available online: https://encyclopedia.pub/entry/4149 (accessed on 27 September 2026).
Xu C. Hypochondrogenesis. Encyclopedia. Available at: https://encyclopedia.pub/entry/4149. Accessed September 27, 2026.
Xu, Camila. "Hypochondrogenesis" Encyclopedia, https://encyclopedia.pub/entry/4149 (accessed September 27, 2026).
Xu, C. (2020, December 23). Hypochondrogenesis. In Encyclopedia. https://encyclopedia.pub/entry/4149
Xu, Camila. "Hypochondrogenesis." Encyclopedia. Web. 23 December, 2020.
Hypochondrogenesis
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This entry is adapted from the peer-reviewed paper https://medlineplus.gov/genetics/condition/hypochondrogenesis

Hypochondrogenesis is a rare, severe disorder of bone growth. This condition is characterized by a small body, short limbs, and abnormal bone formation (ossification) in the spine and pelvis.

genetic conditions

References

  1. Castori M, Brancati F, Scanderbeg AC, Dallapiccola B. Hypochondrogenesis.Pediatr Radiol. 2006 May;36(5):460-1.
  2. Körkkö J, Cohn DH, Ala-Kokko L, Krakow D, Prockop DJ. Widely distributedmutations in the COL2A1 gene produce achondrogenesis type II/hypochondrogenesis. Am J Med Genet. 2000 May 15;92(2):95-100.
  3. Spranger J, Winterpacht A, Zabel B. The type II collagenopathies: a spectrumof chondrodysplasias. Eur J Pediatr. 1994 Feb;153(2):56-65. Review.
  4. Suzumura H, Kohno T, Nishimura G, Watanabe H, Arisaka O. Prenatal diagnosis ofhypochondrogenesis using fetal MRI: a case report. Pediatr Radiol. 2002May;32(5):373-5.
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Subjects: Genetics & Heredity
Contributor MDPI registered users' name will be linked to their SciProfiles pages. To register with us, please refer to https://encyclopedia.pub/register : Camila Xu
View Times: 883
Entry Collection: MedlinePlus
Revision: 1 time (View History)
Update Date: 23 Dec 2020
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