- A dictionary of medical eponyms

Maroteaux-Lamy syndrome II

Related people

A familial form of idiopathic osteolysis, characterized by onset between the ages of 8 and 22 years, slow dissolution of bones of the phalanges of the hands and feet, ulcers of the fingers and soles of the feet, disappearance of bone sequestra, and loss of the digits on healing. A similar condition may be produced on exposure to vinyl chloride. Inheritance is autosomal dominant.

Bibliography

  • P. Maroteaux, M. Lamy:
    Acro-ostéolyse dominante.
    Archives francaises de pédiatrie, Paris, 1961, 18: 693-702.
  • D. K. Harris, W. G. Adams:
    Acro-osteolysis occurring in men engaged in the polymerization of vinyl chloride.
    British Medical Journal, London, 1967, 3: 712-714.

What is an eponym?

An eponym is a word derived from the name of a person, whether real or fictional. A medical eponym is thus any word related to medicine, whose name is derived from a person.

What is Whonamedit?

Whonamedit.com is a biographical dictionary of medical eponyms. It is our ambition to present a complete survey of all medical phenomena named for a person, with a biography of that person.

Disclaimer:

Whonamedit? does not give medical advice.
This survey of medical eponyms and the persons behind them is meant as a general interest site only. No information found here must under any circumstances be used for medical purposes, diagnostically, therapeutically or otherwise. If you, or anybody close to you, is affected, or believe to be affected, by any condition mentioned here: see a doctor.