Proteinuria in a patient with the diaphragmatic hernia-hypertelorism-myopia-deafness syndrome: further evidence that the facio-oculo-acoustico-renal syndrome represents the same entity.

Author:

Devriendt K,Standaert L,Van Hole C,Devlieger H,Fryns J P

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference9 articles.

1. Mendelian inheritance in man. Catalogs of autosomal dominant, autosomal recessive, and X-linked phenotypes;McKusick, V.A.,1992

2. Diaphragmatic hernia, exomphalos, absent corpus callosum, hypertelorism, myopia and sensorineural deafness-a newly recognized autosomal recessive condition?;Donnai, D.; Barrow, M.;Am JMed Genet,1993

3. Syndrome of ocular and facial anomalies, telecanthus and deafness;Holmes, L.B.; Schepens, C.L.;J Pediatr,1972

4. Diaphragmatic herniaexomphalos-hypertelorism syndrome: a new case and further evidence of autosomal recessive inheritance;Gripp, K.W.; Donnai, D.; Clericuzio, C.L.; McDonald-McGinn, D.M.; Guttenberg, M.; Zackai, E.H.;Am J Med Genet,1997

5. Editor's comment;Opitz, J.M.;Am J Med Genet,1997

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