Milroy's diseasen.

Brit.

/ˈmɪlrɔɪz dᵻˌziːz/, U.S.

/ˈmɪlˌrɔɪz dəˌziz/

Origin: From a proper name, combined with an English element. Etymons: proper name Milroy , disease n.

Etymology: < the genitive of the name of William Forsyth Milroy (1855–1942), U.S. physician, who described the disease in 1892 ( N.Y. Med. Jrnl. 56 505) + disease n.

Medicine.

A hereditary (autosomal dominant) form of lymphoedema, in which oedema, particularly involving the lower limbs, is present from birth.

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

1909 W. Osler in W. Osler & T. McCrae Syst. Med. VI. xxviii. 654 Certain persons are born with a special susceptibility to exudative skin lesions. There are families all the members of which present these reactions to particular substances; there are families some members of which are liable to attacks of local œdema, a peculiarity which has been traced through six generations; and lastly, there is an hereditary œdema of the legs (Milroy's disease) which has probably nothing to do with the forms under consideration.

1928 W. F. Milroy in Jrnl. Amer. Med. Assoc. 20 Oct. 1172/2 The condition now under consideration was first designated by my name by Sir William Osler, in his work on the practice of medicine.]

1966 Surgery 60 1098/1 Only a few cases actually qualify as Milroy's disease under the original four points.

1984 J. R. Tighe & D. R. Davies Pathol. (ed. 4) xiii. 116 The most likely clinical examples occur..as a result of congenital absence of lymphatics (Milroy's disease).

1996 Jrnl. Amer. Podiatr. Med. Assoc. 86 400 A pedal complication of Milroy's disease has been presented.

This entry has been updated (OED Third Edition, March 2002; most recently modified version published online March 2022).

单词	milroys disease
释义	Milroy's diseasen. Brit. /ˈmɪlrɔɪz dᵻˌziːz/, U.S. /ˈmɪlˌrɔɪz dəˌziz/ Origin: From a proper name, combined with an English element. Etymons: proper name Milroy , disease n. Etymology: < the genitive of the name of William Forsyth Milroy (1855–1942), U.S. physician, who described the disease in 1892 ( N.Y. Med. Jrnl. 56 505) + disease n. Medicine. A hereditary (autosomal dominant) form of lymphoedema, in which oedema, particularly involving the lower limbs, is present from birth. 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 1909 W. Osler in W. Osler & T. McCrae Syst. Med. VI. xxviii. 654 Certain persons are born with a special susceptibility to exudative skin lesions. There are families all the members of which present these reactions to particular substances; there are families some members of which are liable to attacks of local œdema, a peculiarity which has been traced through six generations; and lastly, there is an hereditary œdema of the legs (Milroy's disease) which has probably nothing to do with the forms under consideration. 1928 W. F. Milroy in Jrnl. Amer. Med. Assoc. 20 Oct. 1172/2 The condition now under consideration was first designated by my name by Sir William Osler, in his work on the practice of medicine.] 1966 Surgery 60 1098/1 Only a few cases actually qualify as Milroy's disease under the original four points. 1984 J. R. Tighe & D. R. Davies Pathol. (ed. 4) xiii. 116 The most likely clinical examples occur..as a result of congenital absence of lymphatics (Milroy's disease). 1996 Jrnl. Amer. Podiatr. Med. Assoc. 86 400 A pedal complication of Milroy's disease has been presented. This entry has been updated (OED Third Edition, March 2002; most recently modified version published online March 2022). < n.1909
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