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Barrett's Esophagus in Rubinstein-Taybi Syndrome
Rubinstein-Taybi syndrome (RSTS; Online Mendelian Inheritance in Man(® )[OMIM(®)] #180849, #613684; Orpha: 783 ) is a rare plurimalformative autosomal dominant genetic disorder that affects one in 100,000-125,000 newborns with equal male and female distribution. It is characterized by distinctive fa...
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| Publicado no: | Cureus |
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| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Cureus
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7769793/ https://ncbi.nlm.nih.gov/pubmed/33391942 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7759/cureus.11709 |
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