Unraveling the mystery: Exploring a case of prolonged fever and hidden genetics: Case report
This case report highlights an unusual presentation of transcobalamin 2 (TCN2) deficiency. It is a rare autosomal recessive disorder. In this case, we present a three-month-old child with prolonged fever and pancytopenia. Initial investigations could not reach a diagnosis. Subsequent investigations...
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| Main Authors: | , , |
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| Format: | Article |
| Language: | English |
| Published: |
Wolters Kluwer Medknow Publications
2025-05-01
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| Series: | Journal of Family Medicine and Primary Care |
| Subjects: | |
| Online Access: | https://journals.lww.com/10.4103/jfmpc.jfmpc_1839_24 |
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