Interstitial lung disease of infancy caused by a new NKX2‐1 mutation
Key Clinical Message Patients with personal or family history of congenital hypothyroidism, and/or neurological findings that also have chronic respiratory symptoms may have a mutation in the NKX2.1 gene as the unifying cause of their disease. Brain–lung–thyroid disease is the ensuing condition, whi...
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| Hlavní autoři: | , , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Wiley
2017-06-01
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| Edice: | Clinical Case Reports |
| Témata: | |
| On-line přístup: | https://doi.org/10.1002/ccr3.901 |
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