Therapeutic Approach of Very Early-Onset Inflammatory Bowel Disease in a Loeys–Dietz Syndrome Child

Heterozygous TGFBR2 loss-of-function mutation is an extremely rare cause of very-early onset inflammatory bowel disease (VEOIBD) as, so far, only three cases have been reported in the literature. VEOIBD therapeutic management remains a real challenge for clinicians. Here, we described an interesting...

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Detalles Bibliográficos
Autores principales: Opréa, Alina, Collardeau-Frachon, Sophie, Heissat, Sophie, Peretti, Noel, Lachaux, Alain, Duclaux-Loras, Rémi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins, Inc. 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10158452/
https://www.ncbi.nlm.nih.gov/pubmed/37168749
http://dx.doi.org/10.1097/PG9.0000000000000139

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10158452/
https://www.ncbi.nlm.nih.gov/pubmed/37168749
http://dx.doi.org/10.1097/PG9.0000000000000139

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