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. Copyright © 2004 Arán Ediciones, S. L.
CITATION STYLE
Rodrigo, L., Riestra, S., Fuentes, D., González, S., López-Vázquez, A., & López-Larrea, C. (2004). Diverse clinical presentations of celiac disease in the same family. Revista Española de Enfermedades Digestivas, 96(9). https://doi.org/10.4321/s1130-01082004000900004
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