Diverse clinical presentations of celiac disease in the same family
We performed a family study to evaluate a total of 34 extended family members (8 siblings, 23 children and nephews, and 3 grandchildren) of an adult patient with celiac disease (CD), a 58- year-old male with severe neurologic involvement manifested as myoclonias. We found 3 other members affected with CD (a 44-year old sister, a 39-year old niece, and a 26-year old nephew). Two of them were completely asymptomatic and all had hypertransaminasemia. All exhibited a villous atrophy pattern of the duodenal mucosa (1 mild, 1 moderate, 1 severe). Overall family involvement was 11.8% (4/14). We wish to emphasize the need to perform extended family studies when diagnosing a case of CD, since risk is not restricted to only first-degree relatives.
Main Authors: | , , , , , |
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Format: | Digital revista |
Language: | English |
Published: |
Sociedad Española de Patología Digestiva
2004
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Online Access: | http://scielo.isciii.es/scielo.php?script=sci_arttext&pid=S1130-01082004000900004 |
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