Research Notes on Three M Syndrome
3-M syndrome (alternative names: dolichospondylic dysplasia, gloomy face syndrome and le Merrer syndrome), is a rare hereditary growth retardation syndrome. The name 3-M originates from the initials of the three authors Miller, McKusick and Malvaux who first reported the syndrome in literature. Major symptoms of 3M syndrome are dwarfism, facial dysmorphia and skeletal abnormalities. No signs of mental retardation are reported. 3-M syndrome is thought to be inherited as an autosomal recessive genetic trait. ...more from Wikipedia
Fast Facts:
Top Resources on Three M Syndrome
- GeneReviews: 3-M Syndrome Summary
- Genetics Home Reference: 3-M Syndrome
- National Organization of Rare Disorders: Three M Syndrome Information
- Madison's Foundation: 3M Dwarfism
- Online Mendelian Inheritance of Man: Three M Syndrome
- WrongDiagnosis: Three M Syndrome Description
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Research Notes References
- ↑ Genetics Home Reference: 3-M Syndrome
- ↑ GeneReviews: 3-M Syndrome Summary
- ↑ Madison's Foundation: 3M Dwarfism
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- Contributor: Jacky Graves
- Reviewer: Chris Miller
- Supervised by: The OrganizedWisdom Physician Review Team
- Last update: Oct. 2, 2008
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