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Description
Kernicterus in an adult who is heterozygous for CriglerNajjar syndrome and homozygous for Gilbert-type genetic defect
Some studies suggest that 10 to 20% of patients continue experiencing symptoms beyond one year despite conservative treatment
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Evid Based Complement Alternat Med2020 Oct 14;2020:4979850
Quick and Painless Our injections are administered using the latest techniques to minimize discomfort
Owing to severe injury or congenital deformity, osteogenesis insufficiency, rheumatoid arthritis or osteoporosis, the long and limited self-healing process of bone grafts cannot fully meet the requirements of timely bone regeneration sometimes [3-5]
