3-M syndrome
3-M syndrome noun: a rare hereditary disorder characterized by severe growth retardation, facial dysmorphia, and skeletal abnormalities.
Noun
3-M syndrome (uncountable)
- A rare hereditary disorder characterized by severe growth retardation, facial dysmorphia, and skeletal abnormalities.
Origin of 3-M syndrome
Derived from the shared surname initial of the three researchers who first identified it in 1972: John D. Miller, an American pediatrician; Victor A. McKusick, an American geneticist; and Paul Malvaux, a Belgian pediatrician.
Questions about 3-M syndrome
- What does 3-M syndrome mean?
- 3-M syndrome means a rare hereditary disorder characterized by severe growth retardation, facial dysmorphia, and skeletal abnormalities.
- What part of speech is 3-M syndrome?
- 3-M syndrome is a noun.
Words near 3-M syndrome in the dictionary
Source and license
Adapted from Wiktionary: 3-M syndrome (page history and authors). Text available under the Creative Commons Attribution-ShareAlike 4.0 license. Word.ws reformatted the entry and added links. Wiktionary data of 2026-09-02.
Last updated:
Cite this entry: “3-M syndrome.” Word.ws, https://word.ws/3-m_syndrome. Based on Wiktionary, CC BY-SA 4.0.
