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In 1974, Lenz and Majewski gave a short description of a 2‐year‐old girl with generalized hyperostosis, proximal symphalangism, syndactyly, brachydactyly, cutis laxa, mental retardation, marked hypertelorism, and enamel hypoplasia. This disorder was later named Lenz–Majewski hyperostotic dwarfism. We describe the reexamination of the original patient at the age of 30 years. Am. J. Med. Genet. 93:335–338, 2000. © 2000 Wiley‐Liss, Inc.
American Journal of Medical Genetics – Wiley
Published: Aug 14, 2000
Keywords: hyperostotic dwarfism; symphalangism; hypertelorism; mental retardation; atrophic skin
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