Cargando…
Intestinal lymphangiectasia in a 3-month-old girl: A case report of Hennekam syndrome caused by CCBE1 mutation
RATIONAL: Intestinal lymphangiectasia (IL) is a rare disease characterized by dilatation and rupture of intestinal lymphatic channels leading to protein-losing enteropathy. IL is classified as primary and secondary types. PATIENT CONCERNS: A 3-month-old girl born at term from vaginal delivery with a...
Autores principales: | Fattorusso, Antonella, Pieri, Elena Sofia, Dell’Isola, Giovanni Battista, Prontera, Paolo, Mencaroni, Elisabetta, Stangoni, Gabriela, Esposito, Susanna |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7337536/ https://www.ncbi.nlm.nih.gov/pubmed/32629717 http://dx.doi.org/10.1097/MD.0000000000020995 |
Ejemplares similares
-
Hennekam lymphangiectasia syndrome
por: Lakshminarayana, G., et al.
Publicado: (2011) -
Novel mutation in CCBE 1 as a cause of recurrent hydrops fetalis from Hennekam lymphangiectasia‐lymphedema syndrome‐1
por: Melber, Dora J., et al.
Publicado: (2018) -
Autism Spectrum Disorders and the Gut Microbiota
por: Fattorusso, Antonella, et al.
Publicado: (2019) -
Porencephaly in an Italian neonate with foetal alcohol spectrum disorder: A case report
por: Mencarelli, Annalisa, et al.
Publicado: (2020) -
Expanding the genetic and clinical characteristics of Protocadherin 19 gene mutations
por: Dell’Isola, Giovanni Battista, et al.
Publicado: (2022)