Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: UMLS:C0019209 (
hepatomegaly
)
5,798
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
Common Variable Immunodeficiency (CVID) and
agammaglobulinemia
are two of the main types of symptomatic primary antibody deficiencies. The pathogenic origins of these two diseases are different;
agammaglobulinemia
is a group of inherited disorders that usually are caused by mutations in the gene encoding Bruton Tyrosine Kinase (BTK) protein while CVID is a heterogeneous disorder mainly without monogenic cause. However, both diseases share a characteristic of frequent bacterial infections, a decline in serum immunoglobulin levels, and abnormality in antibody responses. The demographics and immunologic parameters, clinical manifestation, and mortality statistics from 297 patients with CVID and
agammaglobulinemia
followed up over 2 decades in the Children's Medical Center of Iran. Age at onset of symptom in
agammaglobulinemia
was earlier than CVID but the course of disease in CVID patients was longer than
agammaglobulinemia
patients. Pulmonary infections were the most prevalent clinical manifestations in both groups of patients. Lymphadenopathy,
hepatomegaly
, and splenomegaly were significantly higher in CVID patients than
agammaglobulinemia
patients and there was a significant association between these complications and mortality in CVID patients. Among 297 patients, 128 patients (88 CVID and 40
agammaglobulinemia
) deceased. The predominant causes of death in CVID patients were infections, chronic lung disease, and malignancy while in
agammaglobulinemia
patients were infections and respiratory failure. Infections, especially respiratory infections were the most common complication and cause of death in both CVID and
agammaglobulinemia
groups and recent treatment advances even Immunoglobulin replacement cannot completely control these complications. Thus prompt recognition and specific management of these complications are worthwhile.
...
PMID:Comparison of clinical and immunological features and mortality in common variable immunodeficiency and agammaglobulinemia patients. 3105 34