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| 1 | Catherine Yang | + 621 word(s) | 621 | 2020-12-15 07:17:05 |
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Yang, C. Baller-Gerold Syndrome. Encyclopedia. Available online: https://encyclopedia.pub/entry/4914 (accessed on 26 September 2026).
Yang C. Baller-Gerold Syndrome. Encyclopedia. Available at: https://encyclopedia.pub/entry/4914. Accessed September 26, 2026.
Yang, Catherine. "Baller-Gerold Syndrome" Encyclopedia, https://encyclopedia.pub/entry/4914 (accessed September 26, 2026).
Yang, C. (2020, December 24). Baller-Gerold Syndrome. In Encyclopedia. https://encyclopedia.pub/entry/4914
Yang, Catherine. "Baller-Gerold Syndrome." Encyclopedia. Web. 24 December, 2020.
Copy Citation
Baller-Gerold syndrome is a rare condition characterized by the premature fusion of certain skull bones (craniosynostosis) and abnormalities of bones in the arms and hands.
genetic conditions
References
- Anyane-Yeboa K, Gunning L, Bloom AD. Baller-Gerold syndromecraniosynostosis-radial aplasia syndrome. Clin Genet. 1980 Feb;17(2):161-6.
- Feingold M, Sklower SL, Willner JP, Desnick RH, Cohen MM.Craniosynostosis-radial aplasia: Baller-Gerold syndrome. Am J Dis Child. 1979Dec;133(12):1279-80.
- Santos de Oliveira R, Lajeunie E, Arnaud E, Renier D. Fetal exposure to sodiumvalproate associated with Baller-Gerold syndrome: case report and review of theliterature. Childs Nerv Syst. 2006 Jan;22(1):90-4.
- Van Maldergem L, Piard J, Larizza L, Wang LL. Baller-Gerold Syndrome. 2007 Aug13 [updated 2018 Apr 19]. 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/NBK1204/
- Van Maldergem L, Siitonen HA, Jalkh N, Chouery E, De Roy M, Delague V, Muenke M, Jabs EW, Cai J, Wang LL, Plon SE, Fourneau C, Kestilä M, Gillerot Y, MégarbanéA, Verloes A. Revisiting the craniosynostosis-radial ray hypoplasia association: Baller-Gerold syndrome caused by mutations in the RECQL4 gene. J Med Genet. 2006 Feb;43(2):148-52.
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