Patau's syndromen.

Brit.

/ˈpataʊz ˌsɪndrəʊm/, U.S.

/ˈpɑtaʊz ˌsɪnˌdroʊm/

Forms:

α. 1900s– Patau's syndrome.

β. 1900s– Patau syndrome.

Origin: From proper names, combined with an English element. Etymons: proper name Patau , syndrome n.

Etymology: < the genitive of the name of Klaus Patau, German-born U.S. geneticist (d. c1977), who with others described the condition in 1960 ( Lancet 9 Apr. 790) + syndrome n. In β forms < Patau + syndrome n.

Medicine.

A constellation of congenital anomalies caused by trisomy of chromosome 13, including microcephaly, coloboma of the iris, cleft palate and lip, and malformations of other organs, usually resulting in death within the first year of life.

ΘΚΠ

the world > health and disease > ill health > a disease > congenital or hereditary syndromes > [noun]

amyelia1865

amelia1872

congenital myotonia1886

myotonia congenita1887

Thomsen's disease1890

von Recklinghausen's disease1899

pseudoxanthoma1900

Werdnig–Hoffmann1903

myotonia atrophica1908

Fröhlich1909

Milroy's disease1909

Lindau disease1928

Steinert's disease1932

von Hippel–Lindau disease1932

Werner's syndrome1934

Sturge–Weber syndrome1935

gargoylism1936

Morgagni's syndrome1936

Hurler's disease1937

von Willebrand1941

Turner1942

autism1944

hypophosphatasia1948

Klinefelter1950

mucopolysaccharidosis1952

progeria1957

Pendred1960

Down's syndrome1961

Patau's syndrome1961

Marinesco–Sjögren syndrome1962

cri du chat syndrome1964

Prader–Willi syndrome1964

Noonan syndrome1965

Lesch-Nyhan syndrome1966

Wernicke–Korsakoff1966

Down1967

mannosidosis1969

mucolipidosis1970

Asperger's syndrome1971

Angelman syndrome1972

adrenoleukodystrophy1973

SCID1973

severe combined immune deficiency1973

Miller–Dieker syndrome1980

Asperger1988

Asperger's disorder1994

1961 H. Braga in Lancet 18 Nov. 1147/1 The nomenclature of specific clinical syndromes due to chromosomal aberrations ought to be uniform... It is my impression that the best way would be to call them by the name of the main authors involved: trisomic 17–18 would be called Edwards' syndrome, trisomic 13–15 Patau's syndrome, and so on.

1971 M. Levitan & A. Montagu Textbk. Human Genetics iii. 76 (caption) The shortness of the neck and low-set malformed ears are also found frequently in the Patau (D₁) syndrome.

1978 D. A. P. Evans in R. B. Scott Price's Textbk. Pract. Med. (ed. 12) iv. 354/2 Mongolism (Down's syndrome) is caused by trisomy 21 and the much rarer Edwards and Patau syndromes..by trisomy 18 and 13 respectively.

1995 Independent 26 Dec. 9/1 They had decided to have the tests. They revealed a yet more severe abnormality in their unborn child: Patau's syndrome.

This entry has been updated (OED Third Edition, June 2005; most recently modified version published online March 2022).

单词	pataus syndrome
释义	Patau's syndromen. Brit. /ˈpataʊz ˌsɪndrəʊm/, U.S. /ˈpɑtaʊz ˌsɪnˌdroʊm/ Forms: α. 1900s– Patau's syndrome. β. 1900s– Patau syndrome. Origin: From proper names, combined with an English element. Etymons: proper name Patau , syndrome n. Etymology: < the genitive of the name of Klaus Patau, German-born U.S. geneticist (d. c1977), who with others described the condition in 1960 ( Lancet 9 Apr. 790) + syndrome n. In β forms < Patau + syndrome n. Medicine. A constellation of congenital anomalies caused by trisomy of chromosome 13, including microcephaly, coloboma of the iris, cleft palate and lip, and malformations of other organs, usually resulting in death within the first year of life. ΘΚΠ the world > health and disease > ill health > a disease > congenital or hereditary syndromes > [noun] amyelia1865 amelia1872 congenital myotonia1886 myotonia congenita1887 Thomsen's disease1890 von Recklinghausen's disease1899 pseudoxanthoma1900 Werdnig–Hoffmann1903 myotonia atrophica1908 Fröhlich1909 Milroy's disease1909 Lindau disease1928 Steinert's disease1932 von Hippel–Lindau disease1932 Werner's syndrome1934 Sturge–Weber syndrome1935 gargoylism1936 Morgagni's syndrome1936 Hurler's disease1937 von Willebrand1941 Turner1942 autism1944 hypophosphatasia1948 Klinefelter1950 mucopolysaccharidosis1952 progeria1957 Pendred1960 Down's syndrome1961 Patau's syndrome1961 Marinesco–Sjögren syndrome1962 cri du chat syndrome1964 Prader–Willi syndrome1964 Noonan syndrome1965 Lesch-Nyhan syndrome1966 Wernicke–Korsakoff1966 Down1967 mannosidosis1969 mucolipidosis1970 Asperger's syndrome1971 Angelman syndrome1972 adrenoleukodystrophy1973 SCID1973 severe combined immune deficiency1973 Miller–Dieker syndrome1980 Asperger1988 Asperger's disorder1994 1961 H. Braga in Lancet 18 Nov. 1147/1 The nomenclature of specific clinical syndromes due to chromosomal aberrations ought to be uniform... It is my impression that the best way would be to call them by the name of the main authors involved: trisomic 17–18 would be called Edwards' syndrome, trisomic 13–15 Patau's syndrome, and so on. 1971 M. Levitan & A. Montagu Textbk. Human Genetics iii. 76 (caption) The shortness of the neck and low-set malformed ears are also found frequently in the Patau (D₁) syndrome. 1978 D. A. P. Evans in R. B. Scott Price's Textbk. Pract. Med. (ed. 12) iv. 354/2 Mongolism (Down's syndrome) is caused by trisomy 21 and the much rarer Edwards and Patau syndromes..by trisomy 18 and 13 respectively. 1995 Independent 26 Dec. 9/1 They had decided to have the tests. They revealed a yet more severe abnormality in their unborn child: Patau's syndrome. This entry has been updated (OED Third Edition, June 2005; most recently modified version published online March 2022). < n.1961
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