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Evaluation of the Neurodevelopmental Status for Urea Cycle Disorders: Based on Clinical Experience

dc.authoridTEKMENURAY-UNAL, AYSEL/0000-0001-8730-3968
dc.authoridBozaci, Ayse Ergul/0000-0002-9783-1016
dc.authoridMutlu Albayrak, Hatice/0000-0001-5624-3878
dc.authorscopusid57201619907
dc.authorscopusid57963234400
dc.authorscopusid57879099300
dc.authorscopusid57192270096
dc.authorscopusid57464245200
dc.authorscopusid18233751800
dc.authorscopusid57206379419
dc.authorwosidOzbek, mehmetnuri/LNR-5794-2024
dc.authorwosidtaş, ibrahim/ABG-8476-2020
dc.authorwosidBozaci, Ergul/JBJ-5349-2023
dc.authorwosidTEKMENURAY-UNAL, AYSEL/IWM-4732-2023
dc.authorwosidMutlu Albayrak, Hatice/A-3635-2017
dc.contributor.authorBozaci, Ayse Ergul
dc.contributor.authorGoksoy, Emine
dc.contributor.authorUnal, Aysel Tekmenuray
dc.contributor.authorAlbayrak, Hatice Mutlu
dc.contributor.authorTas, Ibrahim
dc.contributor.authorKanar, Berat
dc.contributor.authorKose, Melis
dc.date.accessioned2025-02-15T19:33:56Z
dc.date.available2025-02-15T19:33:56Z
dc.date.issued2023
dc.departmentArtuklu Universityen_US
dc.department-temp[Bozaci, Ayse Ergul; Tas, Ibrahim] Diyarbakir Childrens Hosp, Clin Pediat Nutr & Metab, Diyarbakir, Turkiye; [Goksoy, Emine] Gaziantep Cengiz Gokcek Obstet & Gynecol & Childre, Clin Pediat Nutr & Metab, Gaziantep, Turkiye; [Unal, Aysel Tekmenuray] Univ Hlth Sci Turkey, Diyarbakir Gaziyaşargil Training & Res Hosp, Clin Med Genet, Diyarbakir, Turkiye; [Albayrak, Hatice Mutlu] Gaziantep Childrens Hosp, Pediat Neurol Clin, Gaziantep, Turkiye; [Kanar, Berat] Diyarbakir Childrens Hosp, Clin Neonatol, Diyarbakir, Turkiye; [Ozbek, Mehmet Nuri] Mardin Artuklu Univ, Dept Pediat, Div Pediat Endocrinol & Metab, Fac Med, Mardin, Turkiye; [Kose, Melis] Childrens Hosp Philadelphia, Mitochondrial Med Frontier Program, Philadelphia, PA USA; [Bozaci, Ayse Ergul] Manisa City Hosp, Div Pediat Endocrinol, Manisa, Turkiyeen_US
dc.descriptionTEKMENURAY-UNAL, AYSEL/0000-0001-8730-3968; Bozaci, Ayse Ergul/0000-0002-9783-1016; Mutlu Albayrak, Hatice/0000-0001-5624-3878en_US
dc.description.abstractAim: Urea cycle disorders (UCD) still have poor neurological outcomes despite early diagnosis and treatment. We aimed to present the neurological outcomes of UCD patients and to determine the main simple and accessible factors affecting these outcomes. Materials and Metkods: This was a descriptive cross-sectional study conducted in two pediatric metabolism centers on 29 patients from 25 unrelated families who were diagnosed and followed with UCD based on clinical presentation, neurological parameters, biochemical measurements, and molecular analysis.Results: Within the study population, the most common diagnosis was argininosuccinate synthase deficiency in 13 (44.82%) patients, followed by N-acetylglutamate synthase deficiency in five patients (17.24%), ornithine transcarbamylase deficiency in four patients (13.79%), arginase 1 deficiency in three patients (10.34%), carbamoyl phosphate synthase 1 deficiency in three patients (10.34%), and argininosuccinate lyase deficiency in one patient (3.44%). Peak ammonia levels were observed to be significantly higher in those patients with delayed milestones and patients who had Denver II <-2 standard deviation score results (p=0.032, p=0.026). Effect sizes were large in both groups. Delayed milestones were noted in 17 (94.4%) of the cases with peak ammonia >500 mu mol/L (n=18). Those patients with abnormal neurological parameters had a significantly higher mean number of hyperammonemic episodes per year. Extracorporeal detoxification was given to eight patients, in combination with therapeutic hypothermia in two patients. Rapid regression was observed in brain edema in those who underwent therapeutic hypothermia.Conclusion: Our study emphasizes the effect of peak ammonia levels and the frequency of hyperammonemic episodes on neurological outcomes. There were still poor neurocognitive outcomes despite extracorporeal detoxification. This highlights the need to reassess current treatment strategies, including the threshold for starting extracorporeal detoxification if ammonia levels exceed 500 mu mol/L. The use of therapeutic hypothermia by experienced teams may be promising due to its brain edema-reducing effects.en_US
dc.description.provenanceSubmitted by GCRIS Admin (gcris@artuklu.edu.tr) on 2025-02-15T19:33:56Z No. of bitstreams: 0en
dc.description.provenanceMade available in DSpace on 2025-02-15T19:33:56Z (GMT). No. of bitstreams: 0 Previous issue date: 2023en
dc.description.woscitationindexEmerging Sources Citation Index
dc.identifier.citationcount0
dc.identifier.doi10.4274/jpr.galenos.2023.96992
dc.identifier.issn2147-9445
dc.identifier.issue3en_US
dc.identifier.scopus2-s2.0-85208449663
dc.identifier.scopusqualityN/A
dc.identifier.urihttps://doi.org/10.4274/jpr.galenos.2023.96992
dc.identifier.urihttps://hdl.handle.net/20.500.12514/5944
dc.identifier.volume10en_US
dc.identifier.wosWOS:001144653500007
dc.language.isoenen_US
dc.publisherGalenos Publ Houseen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectUrea Cycle Disordersen_US
dc.subjectHyperammonemiaen_US
dc.subjectCitrullinemiaen_US
dc.subjectInborn Errors Of Metabolismen_US
dc.subjectTherapeutic Hypothermiaen_US
dc.titleEvaluation of the Neurodevelopmental Status for Urea Cycle Disorders: Based on Clinical Experienceen_US
dc.typeArticleen_US
dspace.entity.typePublication

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