Two distinct clinical progressions of P67phox-deficient CGD, both commencing with cervical lymphadenitis
Abstract We present two rare cases of p67phox-deficient chronic granulomatous disease (CGD) caused by compound heterozygous mutations in the NCF2 gene. They developed cervical lymphadenitis as the initial manifestation of CGD but had distinct clinical progressions. Patient 1 presented with aspergill...
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| Main Authors: | , , , , , |
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| Format: | Book |
| Published: |
BMC,
2024-11-01T00:00:00Z.
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| Online Access: | Connect to this object online. |
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Internet
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| Call Number: |
A1234.567 |
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| Copy 1 | Available |