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Petrus Johannes Waardenburg

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honorary member of these two societies. He also became honorary member of similar Danish, Italian, and German societies. He was made honorary doctor of the Rijksuniversiteit in Leiden in 1954 and of the Wilhelms Universitat of Munster in 1964. Waardenburg spoke out against the use of eugenics to justify racial genocide by Nazis during their occupation of Netherlands from 1940-1945. They allowed him to continue his research because it did often support Nazi ideology.
360:"A new syndrome combining developmental anomalies of the eyelids, eyebrows and noseroot with pigmentary anomalies of the iris and head hair and with congenital deafness; Dystopia canthi medialis et punctorum lacrimalium lateroversa, hyperplasia supercilii medialis et radicis nasi, heterochromia iridum totaliis sive partialis, albinismus circumscriptus (leucismus, polioss) et surditas congenita (surdimutitas)" 148:
From 1934 to 1940, Waardenburg was external university lecturer in medical genetics at Utrecht University. From 1931 to 1935 he was secretary of the Netherlands Ophthalmological Society. He was a founding member of the Netherlands Anthropogenetic Society and its president from 1949 to 1963. He became
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presented a deaf mute child, who was 10 years of age, and had partial albinism of the hair and body, blue hypoplastic rides, blepharophimosis, and malformation of the arms, to the Swiss Society of Genetics, and gave a full report of his findings in 1950. Waardenburg gave an account of a deaf adult
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Waardenburg was almost 50 years of age before he was habilitated as a lecturer in human genetics. At the age of 66, in 1952, he was finally appointed professor of genetics at the Institute of Preventive Medicine, Leiden. Between 1961 and 1974 the three volumes of his book
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Between 1910 and 1970 Waardenburg published 267 papers in all. They included original observations on albinism' and many other hereditary conditions. He contributed the chapter on heredity in eye disease to
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from 1904–11, and then trained in ophthalmology before receiving an MD for a dissertation on the hereditary basis of the physiological and pathological characteristics of the eye in 1913.
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with similar facial features in December 1948, followed by a detailed review in 1951. He described the syndrome as a distinct entity and found the anomalies in 12 of 840 deaf mutes.
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most often characterized by varying degrees of deafness, minor defects in structures arising from the neural crest, and pigmentation anomalies.
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in 1957. He received the Snellen medal in 1959. He founded the Waardenburg prize for special merit in the medical genetic field in 1965.
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observed and described a lateral position of the lacrimal points and shortened eyelid slit in identical deaf mute twins. In August 1947
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were published. Until 1970 Waardenburg gave genetic advice in paternity cases in the Dutch legal courts and genetic counselling.
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might be the consequence of a chromosomal aberration, a fact which was confirmed after 27 years, by
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Waardenburg was a regular contributor to eugenics publications. In 1932 Waardenburg suggested that
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Index

Nijeveen
Utrecht University
Ophthalmologist
geneticist
Waardenburg syndrome
ophthalmologist
geneticist
Waardenburg syndrome
Utrecht University
Down syndrome
Jérôme Lejeune
Waardenburg syndrome
genetic disorder
Jan van der Hoeve
David Klein
Order of the Netherlands Lion
The Neural Crest in Development and Evolution
154
ISBN
0-387-98702-9






"Petrus Johannes Waardenburg, MD"
doi
10.1136/bjo.64.3.224
PMC

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