Distal limb deficiencies, oral involvement, and renal defect: report of a third patient and confirmation of a distinct entity

K Keymolen, R Van Damme-Lombaerts, A Verloes, J P Fryns
American Journal of Medical Genetics 2000 July 3, 93 (1): 19-21
In 1987 Buttiens and Fryns [1987: Am J Med Genet 27:651-660] reported on two sibs, brother and sister, with severe distal limb defects, micrognathia, and mild to moderate mental retardation. The male also showed severe myopia and oligomeganephronia. To the best of our knowledge, no other similar patients have been described since. We report on a boy with a similar phenotype. .

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