Turricephaly is regarded as one of the most challenging cranial malformations to treat because increasing intracranial pressure can occur when cranial height is reduced. In typical medical and nursing situations, kids with turricephaly can be identified by thier osteogenesis imperfecta, ophthalmic proptosis, hydrocephalus, and certain facial characteristics such substantial temporal steamrolling, facial asymmetry hypoplasia, and micrognathia.Turricephaly is a rare and potentially fatal autoimmune disease. In the beginning, estimates of turricephaly from antiquity to the present are shown, and in the end, the findings of a personal investigation into the generally disturbed social behaviour and A 4 year male child admited in pediatric department in hospital the patient reported Head swelling, nausea, occipital area swelling, both eyes swelling, and irregular skull form. the primary therapeutic interventions was given to the patient and he was treated with syp zincovit 5 ml BD antibiotic intravenous fluids during hospitalization and the treatment was continued until my final day of care.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
customersupport@researchsolutions.com
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.