Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
8809147 | Archives de Pédiatrie | 2018 | 6 Pages |
Abstract
TTC7A mutations cause multiple neonatal intestinal atresias with early inflammatory bowel disease and severe combined immunodeficiency. There are no treatment protocols for this rare disease. Two new cases are described for which radical early treatment measures - total enterectomy, home parenteral nutrition, immunoglobulin therapy and intravenous antibiotic prophylaxis - have allowed both patients to develop optimally.
Keywords
Related Topics
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Perinatology, Pediatrics and Child Health
Authors
J. Fayard, S. Collardeau, Y. Bertrand, M.-P. Cordier, C. Malcus, R. Dubois, P.-Y. Mure, G. de Saint Basile, T. Louazon, B. Rohmer, A. Lachaux, R. Duclaux, N. Peretti,