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Xu, C. Hystrix-Like Ichthyosis with Deafness. Encyclopedia. Available online: https://encyclopedia.pub/entry/4245 (accessed on 28 September 2026).
Xu C. Hystrix-Like Ichthyosis with Deafness. Encyclopedia. Available at: https://encyclopedia.pub/entry/4245. Accessed September 28, 2026.
Xu, Camila. "Hystrix-Like Ichthyosis with Deafness" Encyclopedia, https://encyclopedia.pub/entry/4245 (accessed September 28, 2026).
Xu, C. (2020, December 23). Hystrix-Like Ichthyosis with Deafness. In Encyclopedia. https://encyclopedia.pub/entry/4245
Xu, Camila. "Hystrix-Like Ichthyosis with Deafness." Encyclopedia. Web. 23 December, 2020.
Hystrix-Like Ichthyosis with Deafness
Edit
This entry is adapted from the peer-reviewed paper https://medlineplus.gov/genetics/condition/hystrix-like-ichthyosis-with-deafness

Hystrix-like ichthyosis with deafness (HID) is a disorder characterized by dry, scaly skin (ichthyosis) and hearing loss that is usually profound. Hystrix-like means resembling a porcupine; in this type of ichthyosis, the scales may be thick and spiky, giving the appearance of porcupine quills.

genetic conditions

References

  1. Lee JR, White TW. Connexin-26 mutations in deafness and skin disease. ExpertRev Mol Med. 2009 Nov 19;11:e35. doi: 10.1017/S1462399409001276. Review.
  2. Todt I, Hennies HC, Küster W, Smolle J, Rademacher G, Mutze S, Basta D,Eisenschenk A, Ernst A. Neurotological and neuroanatomical changes in theconnexin-26-related HID/KID syndrome. Audiol Neurootol. 2006;11(4):242-8.
  3. van Geel M, van Steensel MA, Küster W, Hennies HC, Happle R, Steijlen PM,König A. HID and KID syndromes are associated with the same connexin 26 mutation.Br J Dermatol. 2002 Jun;146(6):938-42.
  4. van Steensel MA. Gap junction diseases of the skin. Am J Med Genet C Semin MedGenet. 2004 Nov 15;131C(1):12-9. Review. Erratum in: Am J Med Genet C Semin MedGenet. 2006 Feb 15;142(1):58.
  5. Xu J, Nicholson BJ. The role of connexins in ear and skin physiology -functional insights from disease-associated mutations. Biochim Biophys Acta. 2013Jan;1828(1):167-78. doi: 10.1016/j.bbamem.2012.06.024.
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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: 765
Entry Collection: MedlinePlus
Revision: 1 time (View History)
Update Date: 23 Dec 2020
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