Hereditary Angioneurotic Edema and Familial Crohn’s Disease
A 29-year-old man with Crohn’s disease involving the ileum and cecum was seen. He had angioneurotic edema with C-1’ esterase inhibitor deficiency. Later, his 50-year-old mother was evaluated because of abdominal pain. She had recurrent urticaria, C-1’ esterase inhibitor deficiency and radiographic s...
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Format: | Article |
Language: | English |
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Wiley
2000-01-01
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Series: | Canadian Journal of Gastroenterology |
Online Access: | http://dx.doi.org/10.1155/2000/828679 |
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author | Hugh J Freeman |
author_facet | Hugh J Freeman |
author_sort | Hugh J Freeman |
collection | DOAJ |
description | A 29-year-old man with Crohn’s disease involving the ileum and cecum was seen. He had angioneurotic edema with C-1’ esterase inhibitor deficiency. Later, his 50-year-old mother was evaluated because of abdominal pain. She had recurrent urticaria, C-1’ esterase inhibitor deficiency and radiographic studies showed Crohn’s disease of the ileum. A maternal family history revealed other members affected with either Crohn’s disease or angioneurotic edema. The clinical observations in this family suggest that angioneurotic edema associated with C-1’ esterase inhibitor deficiency may be closely linked genetically with a familial form of Crohn’s disease. |
format | Article |
id | doaj-art-b2af8f609563465ab248c8df7f8b6652 |
institution | Kabale University |
issn | 0835-7900 |
language | English |
publishDate | 2000-01-01 |
publisher | Wiley |
record_format | Article |
series | Canadian Journal of Gastroenterology |
spelling | doaj-art-b2af8f609563465ab248c8df7f8b66522025-02-03T01:24:52ZengWileyCanadian Journal of Gastroenterology0835-79002000-01-0114433733910.1155/2000/828679Hereditary Angioneurotic Edema and Familial Crohn’s DiseaseHugh J Freeman0Department of Medicine (Gastroenterology), University of British Columbia, Vancouver, British Columbia, CanadaA 29-year-old man with Crohn’s disease involving the ileum and cecum was seen. He had angioneurotic edema with C-1’ esterase inhibitor deficiency. Later, his 50-year-old mother was evaluated because of abdominal pain. She had recurrent urticaria, C-1’ esterase inhibitor deficiency and radiographic studies showed Crohn’s disease of the ileum. A maternal family history revealed other members affected with either Crohn’s disease or angioneurotic edema. The clinical observations in this family suggest that angioneurotic edema associated with C-1’ esterase inhibitor deficiency may be closely linked genetically with a familial form of Crohn’s disease.http://dx.doi.org/10.1155/2000/828679 |
spellingShingle | Hugh J Freeman Hereditary Angioneurotic Edema and Familial Crohn’s Disease Canadian Journal of Gastroenterology |
title | Hereditary Angioneurotic Edema and Familial Crohn’s Disease |
title_full | Hereditary Angioneurotic Edema and Familial Crohn’s Disease |
title_fullStr | Hereditary Angioneurotic Edema and Familial Crohn’s Disease |
title_full_unstemmed | Hereditary Angioneurotic Edema and Familial Crohn’s Disease |
title_short | Hereditary Angioneurotic Edema and Familial Crohn’s Disease |
title_sort | hereditary angioneurotic edema and familial crohn s disease |
url | http://dx.doi.org/10.1155/2000/828679 |
work_keys_str_mv | AT hughjfreeman hereditaryangioneuroticedemaandfamilialcrohnsdisease |