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Trichohepatoenteric syndrome: A rare mutation in SKIV2L gene in the first Balkan reported case
Trichohepatoenteric syndrome or syndromic diarrhea is a rare and severe Mendelian autosomal recessive syndrome characterized by intractable diarrhea, facial and hair abnormalities, liver dysfunction, immunodeficiency and failure to thrive. It has been associated with mutations in TTC37 and SKIV2L ge...
Autores principales: | Xinias, Ioannis, Mavroudi, Antigoni, Mouselimis, Dimitrios, Tsarouchas, Anastasios, Vasilaki, Konstantina, Roilides, Ioannis, Lacaille, Florence, Giouleme, Olga |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6207980/ https://www.ncbi.nlm.nih.gov/pubmed/30397475 http://dx.doi.org/10.1177/2050313X18807795 |
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