A familial camptodactyly syndrome.
A familial camptodactyly syndrome, transmitted as an autosomal dominant trait, associated with dysplasia and synostoses of the fingers, wrist, and foot with short middle phalanges; craniofacial anomalies; conductive hearing loss; strabismus; and other defects.
- J. Herrmann:
Symphalangism and brachydactyly syndrome: Report of the WL symphalangism-brachydactyly syndrome: review of the literature and classification.
Birth Defects Original Article Series, New York, 1974, 10 (5): 23-53.
- S. A. Hurvitz, et al:
The facio-audio-symphalangism syndrome: A report of a case and review of the literature.
Clinical Genetics, Copenhagen, 1985, 28: 61-68.
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.
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.