A rare combination of MODY5 and duodenal atresia in a patient: a case report
Abstract Background Maturity-onset diabetes of the young (MODY) is a genetically and clinically heterogeneous group of hereditary diabetes, generally caused by one abnormal gene. MODY5 is caused by mutations of the hepatocyte nuclear factor 1 homeobox β gene (HNF1β), always as a part of Chr17q12 del...
| Main Authors: | , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
BMC
2020-02-01
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| Series: | BMC Medical Genetics |
| Subjects: | |
| Online Access: | https://doi.org/10.1186/s12881-020-0954-0 |