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Pubmed for Handhelds
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Title: An oculocerebrofacial syndrome. Author: Kaufman RL, Rimoin DL, Prensky AL, Sly WS. Journal: Birth Defects Orig Artic Ser; 1971 Feb; 7(1):135-8. PubMed ID: 5006210. Abstract: A syndrome of mental retardation, microcephaly, a mongoloid slant to the palpebral fissures, microcornea, strabismus, myopia, optic atrophy, high-arched palate, preauricular skin tags and small mandible is described in four (including one set of twins) of seven sibs born to unaffected, nonconsanguineous parents of German ancestry. An autosomal recessive mode of inheritance seems most likely.[Abstract] [Full Text] [Related] [New Search]