von Gierken.

Brit.

/vɒn ˈɡɪəkə/,

/fɒn ˈɡɪəkə/, U.S.

/vɑn ˈɡɪrkə/

Etymology: < the name of Edgar O. K. von Gierke (1877–1945), German pathologist.

Pathology.

Used in the possessive (usually as von Gierke's disease) and occasionally attributively to designate a type of glycogen storage disease (described by von Gierke in Beiträge zur path. Anat. 82 (1929) 497), caused by a deficiency of glucose-6-phosphatase and characterized by an enlarged liver, obesity, and stunted growth.

ΘΚΠ

the world > health and disease > ill health > a disease > disorders of internal organs > metabolic disorders > [noun] > other metabolic disorders

xanthomatosis1900

Tay-Sachs1907

ketosis1917

protein shock1917

hyperinsulinism1924

Niemann–Pick1928

tyrosinosis1932

von Gierke's disease1933

phenylketonuria1935

cystic fibrosis1938

mucoviscidosis1945

cystinosis1949

oxalosis1952

McArdle1957

orotic aciduria1959

PKU1961

sphingolipidosis1962

Reye's syndrome1965

Menkes1969

the world > health and disease > ill health > a disease > disorders of internal organs > metabolic disorders > [adjective] > other metabolic disorders

von Gierke1933

ketotic1943

cystinotic1961

orotic aciduric1961

phenylketonuric1961

1933 Brit. Med. Jrnl. 11 Mar. 405/1 During life the presence of von Gierke's glycogenic-accumulation disease is not likely to be absolutely established except by the microscopical examination of an excised piece of the liver or material obtained by liver puncture.

1933 Proc. Royal Soc. Med. 26 1006 (heading) Hepatomegaly of unknown origin (probably von Gierke's disease).

1936 Brit. Med. Jrnl. 22 Feb. 361/2 Unshelm..showed that if normal glycogen-free liver was minced up with von Gierke liver and allowed to incubate, the glycogen was broken down.

1952 Metabolism I. 293 The present report is based on studies carried out on a 20-month-old girl with glycogen storage disease of the classical von Gierke type.

1961 R. D. Baker Essent. Pathol. xiv. 344 In some few cases glycogen infiltration of the myocardium is present and the condition is a part of glycogen storage or Von Gierke's disease.

1982 R. A. Lawson et al. Pathologic Mechanisms & Human Dis. ii. 22/1 The glycogen stores are metabolically unavailable, and patients with von Gierke's disease suffer from hypoglycemia.

This entry has not yet been fully updated (first published 1993; most recently modified version published online December 2021).

单词	von gierke
释义	von Gierken. Brit. /vɒn ˈɡɪəkə/, /fɒn ˈɡɪəkə/, U.S. /vɑn ˈɡɪrkə/ Etymology: < the name of Edgar O. K. von Gierke (1877–1945), German pathologist. Pathology. Used in the possessive (usually as von Gierke's disease) and occasionally attributively to designate a type of glycogen storage disease (described by von Gierke in Beiträge zur path. Anat. 82 (1929) 497), caused by a deficiency of glucose-6-phosphatase and characterized by an enlarged liver, obesity, and stunted growth. ΘΚΠ the world > health and disease > ill health > a disease > disorders of internal organs > metabolic disorders > [noun] > other metabolic disorders xanthomatosis1900 Tay-Sachs1907 ketosis1917 protein shock1917 hyperinsulinism1924 Niemann–Pick1928 tyrosinosis1932 von Gierke's disease1933 phenylketonuria1935 cystic fibrosis1938 mucoviscidosis1945 cystinosis1949 oxalosis1952 McArdle1957 orotic aciduria1959 PKU1961 sphingolipidosis1962 Reye's syndrome1965 Menkes1969 the world > health and disease > ill health > a disease > disorders of internal organs > metabolic disorders > [adjective] > other metabolic disorders von Gierke1933 ketotic1943 cystinotic1961 orotic aciduric1961 phenylketonuric1961 1933 Brit. Med. Jrnl. 11 Mar. 405/1 During life the presence of von Gierke's glycogenic-accumulation disease is not likely to be absolutely established except by the microscopical examination of an excised piece of the liver or material obtained by liver puncture. 1933 Proc. Royal Soc. Med. 26 1006 (heading) Hepatomegaly of unknown origin (probably von Gierke's disease). 1936 Brit. Med. Jrnl. 22 Feb. 361/2 Unshelm..showed that if normal glycogen-free liver was minced up with von Gierke liver and allowed to incubate, the glycogen was broken down. 1952 Metabolism I. 293 The present report is based on studies carried out on a 20-month-old girl with glycogen storage disease of the classical von Gierke type. 1961 R. D. Baker Essent. Pathol. xiv. 344 In some few cases glycogen infiltration of the myocardium is present and the condition is a part of glycogen storage or Von Gierke's disease. 1982 R. A. Lawson et al. Pathologic Mechanisms & Human Dis. ii. 22/1 The glycogen stores are metabolically unavailable, and patients with von Gierke's disease suffer from hypoglycemia. This entry has not yet been fully updated (first published 1993; most recently modified version published online December 2021). < n.1933
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