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| 1 | Camila Xu | + 591 word(s) | 591 | 2020-12-15 07:30:16 |
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Xu, C. MECP2-Related Severe Neonatal Encephalopathy. Encyclopedia. Available online: https://encyclopedia.pub/entry/4554 (accessed on 28 September 2026).
Xu C. MECP2-Related Severe Neonatal Encephalopathy. Encyclopedia. Available at: https://encyclopedia.pub/entry/4554. Accessed September 28, 2026.
Xu, Camila. "MECP2-Related Severe Neonatal Encephalopathy" Encyclopedia, https://encyclopedia.pub/entry/4554 (accessed September 28, 2026).
Xu, C. (2020, December 24). MECP2-Related Severe Neonatal Encephalopathy. In Encyclopedia. https://encyclopedia.pub/entry/4554
Xu, Camila. "MECP2-Related Severe Neonatal Encephalopathy." Encyclopedia. Web. 24 December, 2020.
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MECP2-related severe neonatal encephalopathy is a neurological disorder that primarily affects males and causes brain dysfunction (encephalopathy).
genetic conditions
References
- Bianciardi L, Fichera M, Failla P, Di Marco C, Grozeva D, Mencarelli MA, SpigaO, Mari F, Meloni I, Raymond L, Renieri A, Romano C, Ariani F. MECP2 missensemutations outside the canonical MBD and TRD domains in males with intellectualdisability. J Hum Genet. 2016 Feb;61(2):95-101. doi: 10.1038/jhg.2015.118.
- Francke U. Mechanisms of disease: neurogenetics of MeCP2 deficiency. Nat Clin Pract Neurol. 2006 Apr;2(4):212-21. Review.
- Gonzales ML, LaSalle JM. The role of MeCP2 in brain development andneurodevelopmental disorders. Curr Psychiatry Rep. 2010 Apr;12(2):127-34. doi:10.1007/s11920-010-0097-7. Review.
- Kankirawatana P, Leonard H, Ellaway C, Scurlock J, Mansour A, Makris CM, Dure LS 4th, Friez M, Lane J, Kiraly-Borri C, Fabian V, Davis M, Jackson J,Christodoulou J, Kaufmann WE, Ravine D, Percy AK. Early progressiveencephalopathy in boys and MECP2 mutations. Neurology. 2006 Jul 11;67(1):164-6.
- Schüle B, Armstrong DD, Vogel H, Oviedo A, Francke U. Severe congenitalencephalopathy caused by MECP2 null mutations in males: central hypoxia andreduced neuronal dendritic structure. Clin Genet. 2008 Aug;74(2):116-26. doi:10.1111/j.1399-0004.2008.01005.x.
- Villard L. MECP2 mutations in males. J Med Genet. 2007 Jul;44(7):417-23.
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