- A dictionary of medical eponyms

Gilford-Burnier syndrome

Alternative eponyms

  • Burnier’s syndrome
  • Hanhart’s syndrome

Related people

A syndrome characterised by dwarfing, adiposogenital dystrophy and optic atrophy.

Description

A syndrome characterised by dwarfing, adiposogenital dystrophy and optic atrophy. Due to decreased functioning of the anterior pituitary caused by a slow-growing tumour, usually a teratoma, pressing on the pituitary gland. Both sexes affected; age of onset variable. Etiology idiopathic. Autosomal recessive inheritance also well described.

Hanhart's syndrome, or idiopathic hypopituitary dwarfism, is a separate entity. See under Ernst Hanhart, Swiss internist and human geneticist, 1891-1973.

Bibliography

  • H. Gilford:
    Ateliosis: Form of dwarfism.
    Practitioner, London, 1903, 70: 797-819.
  • R. Burnier:
    A new hypophyseal syndrome - hypophyseal nanism.

Annals of Ophthalmology, St. Louis, 1912, 21: 263-274.

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.