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P-021. Jobert syndrome “a rare cause of liver dysfunction”
INTRODUCTION: Joubert syndrome is an autosomal recessive inherited disease with no specific gene mutation. Diagnosis is made by the evaluation of clinical and radiological findings. Coexistence of Joubert syndrome with congenital hepatic fibrosis is called COACH syndrome (Cerebellar vermis hypoplasi...
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| Publicado en: | Turk J Gastroenterol |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Turkish Society of Gastroenterology
2019
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7021083/ https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5152/tjg.2019.27 |
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