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Xu, C. Lenz Microphthalmia Syndrome. Encyclopedia. Available online: https://encyclopedia.pub/entry/4513 (accessed on 26 September 2026).
Xu C. Lenz Microphthalmia Syndrome. Encyclopedia. Available at: https://encyclopedia.pub/entry/4513. Accessed September 26, 2026.
Xu, Camila. "Lenz Microphthalmia Syndrome" Encyclopedia, https://encyclopedia.pub/entry/4513 (accessed September 26, 2026).
Xu, C. (2020, December 23). Lenz Microphthalmia Syndrome. In Encyclopedia. https://encyclopedia.pub/entry/4513
Xu, Camila. "Lenz Microphthalmia Syndrome." Encyclopedia. Web. 23 December, 2020.
Lenz Microphthalmia Syndrome
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This entry is adapted from the peer-reviewed paper https://medlineplus.gov/genetics/condition/lenz-microphthalmia-syndrome

Lenz microphthalmia syndrome is a condition characterized by abnormal development of the eyes and several other parts of the body. It occurs almost exclusively in males.

genetic conditions

References

  1. Forrester S, Kovach MJ, Reynolds NM, Urban R, Kimonis V. Manifestations infour males with and an obligate carrier of the Lenz microphthalmia syndrome. Am JMed Genet. 2001 Jan 1;98(1):92-100. Review.
  2. Ng D, Hadley DW, Tifft CJ, Biesecker LG. Genetic heterogeneity of syndromicX-linked recessive microphthalmia-anophthalmia: is Lenz microphthalmia a singledisorder? Am J Med Genet. 2002 Jul 15;110(4):308-14.
  3. Ng D, Thakker N, Corcoran CM, Donnai D, Perveen R, Schneider A, Hadley DW,Tifft C, Zhang L, Wilkie AO, van der Smagt JJ, Gorlin RJ, Burgess SM, BardwellVJ, Black GC, Biesecker LG. Oculofaciocardiodental and Lenz microphthalmiasyndromes result from distinct classes of mutations in BCOR. Nat Genet. 2004Apr;36(4):411-6.
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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: 947
Entry Collection: MedlinePlus
Revision: 1 time (View History)
Update Date: 23 Dec 2020
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