Congenital isolated adrenocorticotropic hormone deficiency in a newborn caused by TBX19 mutation: a case report and literature review
BackgroundTo investigate the clinical phenotype, genetic characteristics, and prognosis of isolated adrenocorticotropic hormone deficiency in a newborn (IAD, OMIM 201400) caused by mutation of the TBX19 gene.Case presentationThe clinical features, diagnosis, treatment, and prognosis of a newborn wit...
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| Main Authors: | , , |
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| Format: | Book |
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Frontiers Media S.A.,
2024-11-01T00:00:00Z.
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Internet
Connect to this object online.3rd Floor Main Library
| Call Number: |
A1234.567 |
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| Copy 1 | Available |