3-M syndrome

短语

释义与例句

n.
  1. 1.

    A rare hereditary disorder characterized by severe growth retardation, facial dysmorphia, and skeletal abnormalities.

    不可数

词源

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.

来源：wiktionary