Oculopharyngeal muscular dystrophy as a rare cause of dysphagia

Oculopharyngeal muscular dystrophy (OPMD) is a rare cause for late-onset dysphagia. OPMD normally follows an autosomal dominant inheritance. Herein we describe a rare case of an autosomal recessive inheritance of OPMD. An 80-year-old male presented with progressive dysphagia, frequent aspiration and...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:Ann Gastroenterol
Egile Nagusiak: Werling, Sarah, Schrank, Bertold, Eckardt, Alexander J., Hauburger, Anja, Deschauer, Marcus, Müller, Michaela
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Hellenic Society of Gastroenterology 2015
Gaiak:
Case Report
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC4367226/
https://ncbi.nlm.nih.gov/pubmed/25831437
Etiketak: Etiketa erantsi
Etiketarik gabe, Izan zaitez lehena erregistro honi etiketa jartzen!

Antzeko izenburuak