Mycoplasma pneumonia in a patient with X-linked agammaglobulinemia

X-linked agammaglobulinemia (XLA), also referred to as Bruton's tyrosine kinase deficiency, is a rare genetic disorder that affects the immune system. We conducted genetic analysis on patients suffering from immunodeficiency by utilizing Next-Generation Sequencing techniques, as well as their c...

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Veröffentlicht in:	BMC infectious diseases 2024-09, Vol.24 (1), p.972-5, Article 972
Hauptverfasser:	Dai, Bowen, Han, Shujuan, Shen, Yuanfang, Li, Zhi, Chen, Shouhang, Wang, Zhuangzhuang, Yuan, Yan, Zhang, Ruyu, Wang, Chenyu, Zheng, Jiaying, Liang, Qiujing, Wang, Qingmei, Zhang, Yaodong, Zhang, Xiaolong, Wang, Fang, Jin, Yuefei
Format:	Artikel
Sprache:	eng
Schlagworte:	Adult Agammaglobulinaemia Tyrosine Kinase - genetics Agammaglobulinemia Agammaglobulinemia - complications Agammaglobulinemia - genetics Antibiotics Bacterial infections Case studies Clinical outcomes Ear diseases Encephalitis Families & family life Family medical history Fever Gene sequencing Genetic analysis Genetic counseling Genetic Diseases, X-Linked - complications Genetic Diseases, X-Linked - genetics Genetic disorders Genetic screening High-Throughput Nucleotide Sequencing Humans Immune system Immunodeficiency Immunoglobulins Influenza Kinases Male Meningitis Mutation Mycoplasma pneumonia Mycoplasma pneumoniae - genetics Mycoplasma pneumoniae - isolation & purification Next-generation sequencing Patients Pneumonia Pneumonia, Mycoplasma - complications Pneumonia, Mycoplasma - microbiology Primary immunodeficiency Quality of life Sinusitis Steroids Streptococcus infections Tyrosine Viral infections Viruses X-linked agammaglobulinemia
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Beschreibung
Zusammenfassung:	X-linked agammaglobulinemia (XLA), also referred to as Bruton's tyrosine kinase deficiency, is a rare genetic disorder that affects the immune system. We conducted genetic analysis on patients suffering from immunodeficiency by utilizing Next-Generation Sequencing techniques, as well as their closest relatives, to facilitate accurate diagnosis, offer genetic counseling services, and enhance our comprehension of XLA.
ISSN:	1471-2334 1471-2334
DOI:	10.1186/s12879-024-09743-w