Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 1 de 1
Filter
Add more filters










Database
Language
Publication year range
1.
Saudi J Gastroenterol ; 23(3): 206-208, 2017.
Article in English | MEDLINE | ID: mdl-28611345

ABSTRACT

Neuroblastoma amplified sequence (NBAS) gene mutation or infantile liver failure syndrome type 2 (ILFS type 2) is an extremely rare disease characterized by episodic liver failure precipitated by intercurrent febrile illness, and liver function recovering completely. Here, we report a 4-year-old girl with recurrent hepatitis. A diagnosis of ILFS type 2 was made based on NBAS mutation gene found by whole-exome sequencing. Our case provides a new insight toward considering NBAS mutation as a part of the differential diagnoses of any infant presenting with recurrent liver failure or hepatitis. We recommend sequencing NBAS in cases of recurrent hepatitis in infancy of unknown cause, especially in individuals with fever-associated hepatic dysfunction.


Subject(s)
Hepatitis/diagnosis , Hepatitis/genetics , Liver Failure/diagnosis , Liver Failure/genetics , Mutation , Neoplasm Proteins/genetics , Child, Preschool , Diagnosis, Differential , Female , Humans , Liver Failure/pathology , Neoplasm Proteins/deficiency , Rare Diseases , Recurrence , Exome Sequencing/methods
SELECTION OF CITATIONS
SEARCH DETAIL