Dealing with congenital hepatic fibrosis? Remember COACH syndrome
Author:
Publisher
Springer Science and Business Media LLC
Subject
Gastroenterology,General Medicine
Link
http://link.springer.com/content/pdf/10.1007/s12328-013-0418-6.pdf
Reference9 articles.
1. Hunter AGW, Rothman SJ, Hwang WS, et al. Hepatic fibrosis, polycystic kidney, colobomata and encephalopathy in siblings. Clin Genet. 1974;6:82–9.
2. Thompson E, Baraitser M. An autosomal recessive mental retardation syndrome with hepatic fibrosis and renal cysts. Am J Med Genet. 1986;24:151–8.
3. Verloes A, Lambotte C. Further delineation of syndrome of cerebellar vermis aplasia/hypoplasia, oligophrenia, congenital ataxia, coloboma and hepatic fibrosis. Am J Med Genet. 1989;32:127–32.
4. Mitsui F, Aikata H, Azakami T, et al. The first Japanese case of COACH Syndrome. Hepat Res. 2009;39:318–23.
5. Doherty D, Parisi MA, Finn LS, et al. Mutations in 3 genes(MKS3, CC2D2Aand RPGRIP1L) cause COACH syndrome. (Joubert Syndrome with congenital hepatic fibrosis). J Med Genet. 2010;4:8–21.
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