Context: The clinical and laboratory features of dominant acute hepatic porphyrias (AHPs) in prepubertal children and adolescents have not been well established.
Objective: To evaluate clinical and laboratory features of AHPs in prepubertal children and adolescents compared to adults.
Data sources: OVID (Embase Classic+Embase and MEDLINE), Scopus, and Google Scholar.
Study selection: Studies describing symptomatic children or adolescents (<18 years old) with increased urinary porphobilinogen were included.
Data extraction: Two reviewers independently extracted the data, with a third reviewer arbitrating discrepancies.
Results: 100 studies were included describing 112 patients (26 prepubertal children and 86 adolescents). Differences were found between prepubertal children and adolescents regarding sex distribution (female-to-male ratio: 1:2 vs. 4:1), clinical manifestations, and concomitant clinical manifestations.
Limitations: There was variation in the methods used to diagnose porphyria attacks across studies, and some elements of the quality of individual studies were unclear.
Conclusions: Prepubertal children with AHPs and porphyria attacks presented with distinct demographic and clinical characteristics from adolescents and adults. Nearly two-thirds of the affected children were males, and about half had a concomitant medical condition that can constitutively upregulate hepatic δ-aminolevulinic acid synthase-1. Adolescents were comparable to adults in almost all respects.
Keywords: Abdominal pain; Adolescent; Child; Epilepsy; Neurologic manifestations; Pediatrics; Porphobilinogen; Porphyrias; Puberty; Seizures.
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