Inborn errors of immunity (IEI) are a heterogeneous group of diseases with variable clinical phenotypes. Without the IEI national registry, this study has been conducted to describe the epidemiology, clinical presentations, treatment, and outcome of IEI in Jordanian children.
MethodsRetrospective data analysis for IEI children diagnosed and followed in Immunology, Allergy, and Rheumatology Division Queen Rania Children's Hospital, the only pediatric hospital in Jordan from 2010 till the end of 2022.
ResultsA total of 467 patients, 263 (56.3%) males and 204 (43.7%) females, were diagnosed with IEI. The prevalence of IEI was 16.2/100,000 Jordanian children. The mean age at symptom onset was 18 months (1 week to 144 months), a positive family history was reported in 43.5%, and the consanguinity rate was 47.9%. The most common IEI category was immunode ciencies affecting cellular and humoral immunity at 33.2%, followed by predominantly antibody de ciencies (PAD) at 16.9%. The overall IEI diagnostic delay mean (range) was 12.6 (0-135) months. Pulmonary and gastrointestinal clinical features were the most common at 55.2% and 45.6%, respectively; the majority were infection-related. The overall mortality was 33.2%; the highest rate was reported in severe combined immunode ciency (SCID) at 56.2%
ConclusionsThe high minimal estimated IEI prevalence at 16.2/100,000 Jordanian children compared to the regional and worldwide data, with the diversities in clinical presentation and distribution of IEI categories in our cohort point to unique features of IEI in Jordanian children, heeding national registry establishment, regional and international collaborative networks.Jordan is an Arab country in the Levant Region of Western Asia, on the East Bank of the Jordan River. Based on the Department of Statistics 2022 data bank, Jordan inhabitants are 11.3 million, 2.9 million are noncitizens (refugees and immigrants), 94% of the Jordanians are Arabs, and the pediatric age group 0-14 years accounts for 34.4% of the population [9]. Consanguineous marriage is widely practiced in Jordan, resembling other Arab communities; even though it has declined from 57-35% over two decades [10], it is still high enough to engender monogenic diseases like IEI. Till now, there is no national IEI registry in Jordan to facilitate epidemiological and clinical data collection and analysis; for this reason, we established a hospital-based database by the Immunology, Allergy, and Rheumatology Division (the only dedicated unit for IEI in the country) at Queen Rania Children's Hospital where all IEI patients had registered since 2010. This study is the rst comprehensive report in Jordan that describes the epidemiology, clinical presentations, treatment, and outcome of Jordanian children with IEI and compares the data to published IEI reports in the region. The previously published PID data in Jordan were either case reports, series, or, within collaborative regional projects, the PAD category in Jordanian children published in 2014 [11].
Methods
Patients and ...