In Pursuit: A Mother’s Account of Her Son’s Rare Disease Diagnosis Journey
A personal account from a mother’s perspective on her undiagnosed son’s medical journey over almost 6 years toward a diagnosis of a rare genetic variant in mitogen-activated protein kinase 8 interacting protein 3 (MAPK8IP3) resulting in neurodevelopment disorder.
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| Format: | Article |
| Language: | English |
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Advocate Aurora Health
2021-10-01
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| Series: | Journal of Patient-Centered Research and Reviews |
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| Online Access: | https://institutionalrepository.aah.org/cgi/viewcontent.cgi?article=1845&context=jpcrr |