Faciocardiorenal syndrome is a rare genetic disorder characterized by facial dysmorphisms, congenital heart defects, and the presence of a horseshoe kidney, alongside intellectual disabilities.[2] Facial dysmorphisms include protruding ears, narrowing of the mouth, cleft palate, hypertelorism, etc.[3] Only 4 cases from the United States,[4] Northern Ireland,[5] and Mexico[6] have been described in the medical literature.[7] Transmission is, presumably, autosomal recessive.[2]
| Faciocardiorenal syndrome | |
|---|---|
| Other names | Eastman Bixler syndrome[1] |
 | |
| Medical genetics | |
References edit
- ^ "Faciocardiorenal syndrome". NORD (National Organization for Rare Disorders). June 16, 2022. Retrieved October 28, 2022.
- ^ a b "Orphanet: Faciocardiorenal syndrome". www.orpha.net. Retrieved October 28, 2022.
- ^ "Faciocardiorenal syndrome – About the Disease – Genetic and Rare Diseases Information Center". rarediseases.info.nih.gov. Retrieved October 28, 2022.
- ^ Eastman, J. R.; Bixler, D. (June 1977). "Facio-cardio-renal syndrome: a newly delineated recessive disorder". Clinical Genetics. 11 (6): 424–430. doi:10.1111/j.1399-0004.1977.tb01339.x. ISSN 0009-9163. PMID 880742. S2CID 26478777.
- ^ Nevin, N. C.; Hill, A. E.; Carson, D. J. (July 1, 1991). "Facio-cardio-renal (Eastman-Bixler) syndrome". American Journal of Medical Genetics. 40 (1): 31–33. doi:10.1002/ajmg.1320400106. ISSN 0148-7299. PMID 1887846.
- ^ Brambila Tapia, A. J. L.; Vásquez Velásque, A. I.; González Mercado, M. G.; Macías Chumacera, A.; Gutierrez-Amavizca, B. E.; Lara Aguilar, R. A.; Pérez Juárez, Canton R.; Moreno Andrade, A.; Figuera, L. E. (2012). "Faciocardiorenal syndrome: a wide clinical spectrum?". Genetic Counseling (Geneva, Switzerland). 23 (1): 51–56. ISSN 1015-8146. PMID 22611642.
- ^ "Entry – 227280 – Faciocardiorenal syndrome – OMIM". omim.org. Retrieved October 28, 2022.
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