Anophthalmia (English Wikipedia)

Wiese, K. Günter; Vogel, Martin; Guthoff, Rudolf; Gundlach, Karsten K.H. (1999). "Treatment of congenital anophthalmos with self-inflating polymer expanders: A new method". Journal of Cranio-Maxillofacial Surgery. 27 (2): 72–6. doi:10.1016/S1010-5182(99)80016-X. PMID 10342141.
Chou CM, Nelson C, Tarle SA, Pribila JT, Bardakjian T, Woods S, Schneider A, Glaser T (2015). "Biochemical Basis for Dominant Inheritance, Variable Penetrance, and Maternal Effects in RBP4 Congenital Disease". Cell. 161 (3): 634–646. doi:10.1016/j.cell.2015.03.006. PMC 4409664. PMID 25910211.
Verma, Amit S; Fitzpatrick, David R (2007). "Anophthalmia and microphthalmia". Orphanet Journal of Rare Diseases. 2: 47. doi:10.1186/1750-1172-2-47. PMC 2246098. PMID 18039390.
Chowdhury, Fuad; Wang, Lei; Al-Raqad, Mohammed; Amor, David J.; Baxová, Alice; Bendová, Šárka; Biamino, Elisa; Brusco, Alfredo; Caluseriu, Oana; Cox, Nancy J.; Froukh, Tawfiq; Gunay-Aygun, Meral; Hančárová, Miroslava; Haynes, Devon; Heide, Solveig (July 2021). "Haploinsufficiency of PRR12 causes a spectrum of neurodevelopmental, eye, and multisystem abnormalities". Genetics in Medicine. 23 (7): 1234–1245. doi:10.1038/s41436-021-01129-6. ISSN 1098-3600. PMID 33824499.
Elliott, J; Maltby, E L; Reynolds, B (1993). "A case of deletion 14(q22.1→q22.3) associated with anophthalmia and pituitary abnormalities". Journal of Medical Genetics. 30 (3): 251–2. doi:10.1136/jmg.30.3.251. PMC 1016311. PMID 7682620.
Schellini, Silvana; El Dib, Regina; Silva, Leandro RE; Farat, Joyce G; Zhang, Yuqing; Jorge, Eliane C (2016-11-07). Cochrane Eyes and Vision Group (ed.). "Integrated versus non-integrated orbital implants for treating anophthalmic sockets". Cochrane Database of Systematic Reviews. 11 (6): CD010293. doi:10.1002/14651858.CD010293.pub2. PMC 6465188. PMID 27820878.
Dharmasena, Aruna; Keenan, Tiarnan; Goldacre, Raph; Hall, Nick; Goldacre, Michael J (2017). "Trends over time in the incidence of congenital anophthalmia, microphthalmia and orbital malformation in England: Database study". British Journal of Ophthalmology. 101 (6): 735–739. doi:10.1136/bjophthalmol-2016-308952. PMID 27601422. S2CID 27880982.
Kataev, MG; Filatova, IA; Verigo, EN; Kiriukhina, SL (2000). "Potentialities of conservative and surgical treatment of patients with congenital microphthalmia and anophthalmia". Vestnik Oftalmologii. 116 (6): 9–13. PMID 11196218.

ncbi.nlm.nih.gov

Chou CM, Nelson C, Tarle SA, Pribila JT, Bardakjian T, Woods S, Schneider A, Glaser T (2015). "Biochemical Basis for Dominant Inheritance, Variable Penetrance, and Maternal Effects in RBP4 Congenital Disease". Cell. 161 (3): 634–646. doi:10.1016/j.cell.2015.03.006. PMC 4409664. PMID 25910211.
Verma, Amit S; Fitzpatrick, David R (2007). "Anophthalmia and microphthalmia". Orphanet Journal of Rare Diseases. 2: 47. doi:10.1186/1750-1172-2-47. PMC 2246098. PMID 18039390.
Elliott, J; Maltby, E L; Reynolds, B (1993). "A case of deletion 14(q22.1→q22.3) associated with anophthalmia and pituitary abnormalities". Journal of Medical Genetics. 30 (3): 251–2. doi:10.1136/jmg.30.3.251. PMC 1016311. PMID 7682620.
Schellini, Silvana; El Dib, Regina; Silva, Leandro RE; Farat, Joyce G; Zhang, Yuqing; Jorge, Eliane C (2016-11-07). Cochrane Eyes and Vision Group (ed.). "Integrated versus non-integrated orbital implants for treating anophthalmic sockets". Cochrane Database of Systematic Reviews. 11 (6): CD010293. doi:10.1002/14651858.CD010293.pub2. PMC 6465188. PMID 27820878.

ghr.nlm.nih.gov

"SOX2 - SRY (sex determining region Y)-box 2 - Genetics Home Reference". Ghr.nlm.nih.gov. 2012-07-09. Retrieved 2012-07-17.

nei.nih.gov

"Anophthalmia and Microphthalmia, Facts About [NEI Health Information]". Nei.nih.gov. Archived from the original on 2012-07-18. Retrieved 2012-07-17.

nypost.com

Steinbuch, Yaron (2024-02-08). "Baby born without eyes due to rare genetic disorder". Retrieved 2024-02-09.

ox.ac.uk

ora.ox.ac.uk

Dharmasena, Aruna; Keenan, Tiarnan; Goldacre, Raph; Hall, Nick; Goldacre, Michael J (2017). "Trends over time in the incidence of congenital anophthalmia, microphthalmia and orbital malformation in England: Database study". British Journal of Ophthalmology. 101 (6): 735–739. doi:10.1136/bjophthalmol-2016-308952. PMID 27601422. S2CID 27880982.

radiopaedia.org

"Anophthalmia | Radiology Reference Article". Radiopaedia.org. Retrieved 2012-07-17.

semanticscholar.org

api.semanticscholar.org

Dharmasena, Aruna; Keenan, Tiarnan; Goldacre, Raph; Hall, Nick; Goldacre, Michael J (2017). "Trends over time in the incidence of congenital anophthalmia, microphthalmia and orbital malformation in England: Database study". British Journal of Ophthalmology. 101 (6): 735–739. doi:10.1136/bjophthalmol-2016-308952. PMID 27601422. S2CID 27880982.

state.mn.us

health.state.mn.us

"MCYSHN: Anophthalmia and Microphthalmia Health Condition Fact Sheet". Health.state.mn.us. 2010-11-16. Archived from the original on 2012-08-07. Retrieved 2012-07-17.

tabanmd.com

"Prosthetic Eye - Fake Eye -Socket Surgery". Tabanmd.com. Retrieved 2012-07-17.

viscotland.org.uk

"anophthalmia". Viscotland.org.uk. Archived from the original on 2012-04-26. Retrieved 2012-07-17.

web.archive.org

"Questions about Anophthalmia". Anophthalmia.org. Archived from the original on 2012-07-28. Retrieved 2012-07-17.
"Summary of Results from Anophthalmia-Microphthalmia Genetics Study". Macs.org.uk. Archived from the original on 2012-07-28. Retrieved 2012-07-17.
"What is Anophthalmia". Macs.org.uk. Archived from the original on 2012-07-28. Retrieved 2012-07-17.
"Anophthalmia and Microphthalmia, Facts About [NEI Health Information]". Nei.nih.gov. Archived from the original on 2012-07-18. Retrieved 2012-07-17.
"ican - the International Children's Anophthalmia Network. Information and support for Anophthalmia, Microphthalmia and Coloboma". Anophthalmia.org. Archived from the original on 2012-07-12. Retrieved 2012-07-17.
"anophthalmia". Viscotland.org.uk. Archived from the original on 2012-04-26. Retrieved 2012-07-17.
"MCYSHN: Anophthalmia and Microphthalmia Health Condition Fact Sheet". Health.state.mn.us. 2010-11-16. Archived from the original on 2012-08-07. Retrieved 2012-07-17.

worldcat.org

Chowdhury, Fuad; Wang, Lei; Al-Raqad, Mohammed; Amor, David J.; Baxová, Alice; Bendová, Šárka; Biamino, Elisa; Brusco, Alfredo; Caluseriu, Oana; Cox, Nancy J.; Froukh, Tawfiq; Gunay-Aygun, Meral; Hančárová, Miroslava; Haynes, Devon; Heide, Solveig (July 2021). "Haploinsufficiency of PRR12 causes a spectrum of neurodevelopmental, eye, and multisystem abnormalities". Genetics in Medicine. 23 (7): 1234–1245. doi:10.1038/s41436-021-01129-6. ISSN 1098-3600. PMID 33824499.