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. 2023 Oct;43(7):1479-1482.
doi: 10.1007/s10875-023-01510-x. Epub 2023 Jun 1.

Inherited STAT1 Deficiency in a Child with BCG-osis and Severe COVID-19 Pneumonia

Mame Sokhna Guèye  1 , Mame Téné Ndiaye-Diop  2   3 ; MSMD Consortium; Jacinta Bustamante #  4   5   6   7 , Tandakha Ndiaye Dièye #  8   9   10
Collaborators, Affiliations

Inherited STAT1 Deficiency in a Child with BCG-osis and Severe COVID-19 Pneumonia

Mame Sokhna Guèye et al. J Clin Immunol. 2023 Oct.
No abstract available

PubMed Disclaimer

Conflict of interest statement

The authors declare no competing interests.

Figures

Fig. 1
Fig. 1
Autosomal recessive partial STAT1 deficiency in Senegal. (A) STAT1 genotype and pedigree of the kindred. The index case is indicated with a black circle. (B) Patient’s chest X-rays (showing a bilateral interstitial pneumonia). (C) Patient’s ethnicity by principal component analysis (PCA). (D) Genomic sequences in the sense orientation of exon 23 of STAT1 (NM_001384891.1) in the index patient, a healthy control and the other family members as indicate in the pedigree. (E) Map of the African countries where MSMD cases have been identified (orange colored countries) and their respective diseases
See this image and copyright information in PMC

References

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