Further delineation of the 3-M syndrome with review of the literature |
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Authors: | R C Hennekam J B Bijlsma J Spranger |
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Affiliation: | Clinical Genetics Center Utrecht, The Netherlands. |
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Abstract: | The 3-M syndrome is a clinically recognizable disorder characterized by prenatal and postnatal growth retardation and a spectrum of consistent minor anomalies. Intelligence seems normal. Inheritance is probably autosomal recessive, with possible expression of the mutant gene in the heterozygote. Three sibs with the 3-M syndrome are reported, together with an extensive review of the pertinent literature. |
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