The 3-M syndrome.
Open Access
- 1 April 1984
- journal article
- case report
- Published by BMJ in Journal of Medical Genetics
- Vol. 21 (2), 124-128
- https://doi.org/10.1136/jmg.21.2.124
Abstract
An interstitial deletion of 16q was identified in an infant with failure to thrive, dysmorphic facies, and congenital heart defects. The mother of this infant had a similar deletion of 16q with ring formation of a fragment presumed to be derived from the deleted portion of 16q. We discuss these cases and compare them to other reports of 16q deletions.Keywords
This publication has 4 references indexed in Scilit:
- 3-M Slender-Boned NanismAmerican Journal of Diseases of Children, 1981
- "New" dwarfing syndromes.1977
- A new familial intrauterine growth retardation syndrome the ?3-M syndrome?European Journal of Nuclear Medicine and Molecular Imaging, 1976
- The 3-M syndrome: a heritable low birthweight dwarfism.1975