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| Version | Summary | Created by | Modification | Content Size | Created at | Operation |
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| 1 | Rita Xu | + 1025 word(s) | 1025 | 2020-12-15 07:33:26 |
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Xu, R. Nonsyndromic Holoprosencephaly. Encyclopedia. Available online: https://encyclopedia.pub/entry/4624 (accessed on 27 September 2026).
Xu R. Nonsyndromic Holoprosencephaly. Encyclopedia. Available at: https://encyclopedia.pub/entry/4624. Accessed September 27, 2026.
Xu, Rita. "Nonsyndromic Holoprosencephaly" Encyclopedia, https://encyclopedia.pub/entry/4624 (accessed September 27, 2026).
Xu, R. (2020, December 24). Nonsyndromic Holoprosencephaly. In Encyclopedia. https://encyclopedia.pub/entry/4624
Xu, Rita. "Nonsyndromic Holoprosencephaly." Encyclopedia. Web. 24 December, 2020.
Copy Citation
Nonsyndromic holoprosencephaly is an abnormality of brain development that also affects the head and face.
genetic conditions
References
- Dubourg C, Bendavid C, Pasquier L, Henry C, Odent S, David V.Holoprosencephaly. Orphanet J Rare Dis. 2007 Feb 2;2:8. Review.
- Fernandes M, Hébert JM. The ups and downs of holoprosencephaly: dorsal versus ventral patterning forces. Clin Genet. 2008 May;73(5):413-23. doi:10.1111/j.1399-0004.2008.00994.x.
- Monuki ES. The morphogen signaling network in forebrain development andholoprosencephaly. J Neuropathol Exp Neurol. 2007 Jul;66(7):566-75. Review.
- Orioli IM, Castilla EE. Epidemiology of holoprosencephaly: Prevalence and riskfactors. Am J Med Genet C Semin Med Genet. 2010 Feb 15;154C(1):13-21. doi:10.1002/ajmg.c.30233. Review.
- Pineda-Alvarez DE, Dubourg C, David V, Roessler E, Muenke M. Currentrecommendations for the molecular evaluation of newly diagnosed holoprosencephalypatients. Am J Med Genet C Semin Med Genet. 2010 Feb 15;154C(1):93-101. doi:10.1002/ajmg.c.30253. Review.
- Roessler E, Muenke M. The molecular genetics of holoprosencephaly. Am J MedGenet C Semin Med Genet. 2010 Feb 15;154C(1):52-61. doi: 10.1002/ajmg.c.30236.Review.
- Solomon BD, Mercier S, Vélez JI, Pineda-Alvarez DE, Wyllie A, Zhou N, Dubourg C, David V, Odent S, Roessler E, Muenke M. Analysis of genotype-phenotypecorrelations in human holoprosencephaly. Am J Med Genet C Semin Med Genet. 2010Feb 15;154C(1):133-41. doi: 10.1002/ajmg.c.30240. Review.
- Solomon BD, Pineda-Alvarez DE, Mercier S, Raam MS, Odent S, Muenke M.Holoprosencephaly flashcards: A summary for the clinician. Am J Med Genet C SeminMed Genet. 2010 Feb 15;154C(1):3-7. doi: 10.1002/ajmg.c.30245. Review.
- Tekendo-Ngongang C, Muenke M, Kruszka P. Holoprosencephaly Overview. 2000 Dec 27 [updated 2020 Mar 5]. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, BeanLJH, Stephens K, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA):University of Washington, Seattle; 1993-2020. Available fromhttp://www.ncbi.nlm.nih.gov/books/NBK1530/
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