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TTC19-related mitochondrial complex III deficiency: Clinical and genetic characterization of 10 patients from 5 unrelated Arab families.

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Title: TTC19-related mitochondrial complex III deficiency: Clinical and genetic characterization of 10 patients from 5 unrelated Arab families.
Authors: Alghamdi M; Division of Medical Genetics, Department of Pediatrics, King Saud University, College of Medicine, Riyadh, Saudi Arabia; Department of Pediatrics, King Saud University Medical City Riyadh, Saudi Arabia. Electronic address: Malghamdi@ksu.edu.sa., Alahmad A; Kuwait Medical Genetics Centre, Ghanima Alghanim Building, Al-Sabah Medical Area, Kuwait., Alaboudi M; Neuromuscular Medicine Center at Case Western University, University Hospitals Cleveland Medical Center, United States of America., Alsheikh S; Department of Neuroradiology, King Fahad Medical City, Altakassusi Alliance Medical, Riyadh, Saudi Arabia., Alanazy MH; Department of Medicine, King Saud University Medical City and College of Medicine, King Saud University, Riyadh, Saudi Arabia., Albash B; Kuwait Medical Genetics Centre, Ghanima Alghanim Building, Al-Sabah Medical Area, Kuwait., Alaqeel A; Department of Paediatrics, Ahmadi Hospital, Kuwait Oil Company (KOC), Kuwait., Almontashiri NA; Center for Genetics and Inherited Diseases (CGID) and Faculty of Applied Medical Science, Taibah University, Madinah, Saudi Arabia., Jamjoom D; Department of Radiology, King Saud University Medical City and College of Medicine, King Saud University, Riyadh, Saudi Arabia., Bashiri FA; Division of Neurology, Department of Pediatric, College of Medicine, King Saud University Medical City, King Saud University, Riyadh, Saudi Arabia., Hamad MH; Division of Neurology, Department of Pediatric, College of Medicine, King Saud University Medical City, King Saud University, Riyadh, Saudi Arabia., Ali HH; Research Center, College of Medicine, King Saud University, Saudi Arabia., Alwatidi M; Research Center, College of Medicine, King Saud University, Saudi Arabia., Alharbi E; Center for Genetics and Inherited Diseases (CGID) and Faculty of Applied Medical Science, Taibah University, Madinah, Saudi Arabia., Omar S; Kuwait Medical Genetic Centre, Ministry of Health, Suliabikhat 80901, Kuwait., Marafi D; Kuwait Medical Genetic Centre, Ministry of Health, Suliabikhat 80901, Kuwait; Department of Pediatrics, College of Medicine, Kuwait University, PO Box 24923, Safat 13110, Kuwait; Department of Pediatrics, Adan Hospital, Ministry of Health, Hadiya 52700, Kuwait., Alabdulrazzaq F; Kuwait Institute for Medical Specialization, Suliabikhat, PO Box 1793, Safat 13018, Kuwait., Arold ST; KAUST Center of Excellence for Smart Health, Biological and Environmental Science and Engineering Division, King Abdullah University of Science and Technology (KAUST), Thuwal 23955-6900, Saudi Arabia., McFarland R; Mitochondrial Research Group, Translational and Clinical Research Institute, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, UK; NHS Highly Specialised Services for Rare Mitochondrial Disorders, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK., W Taylor R; Mitochondrial Research Group, Translational and Clinical Research Institute, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, UK; NHS Highly Specialised Services for Rare Mitochondrial Disorders, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK.
Source: Molecular genetics and metabolism [Mol Genet Metab] 2026 Jun; Vol. 148 (2), pp. 109867. Date of Electronic Publication: 2026 Mar 09.
Publication Type: Journal Article
Journal Info: Publisher: Academic Press Country of Publication: United States NLM ID: 9805456 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1096-7206 (Electronic) Linking ISSN: 10967192 NLM ISO Abbreviation: Mol Genet Metab Subsets: MEDLINE
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  Data: TTC19-related mitochondrial complex III deficiency: Clinical and genetic characterization of 10 patients from 5 unrelated Arab families.
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  Data: <searchLink fieldCode="AU" term="%22Alghamdi+M%22">Alghamdi M</searchLink>; Division of Medical Genetics, Department of Pediatrics, King Saud University, College of Medicine, Riyadh, Saudi Arabia; Department of Pediatrics, King Saud University Medical City Riyadh, Saudi Arabia. Electronic address: Malghamdi@ksu.edu.sa.<br /><searchLink fieldCode="AU" term="%22Alahmad+A%22">Alahmad A</searchLink>; Kuwait Medical Genetics Centre, Ghanima Alghanim Building, Al-Sabah Medical Area, Kuwait.<br /><searchLink fieldCode="AU" term="%22Alaboudi+M%22">Alaboudi M</searchLink>; Neuromuscular Medicine Center at Case Western University, University Hospitals Cleveland Medical Center, United States of America.<br /><searchLink fieldCode="AU" term="%22Alsheikh+S%22">Alsheikh S</searchLink>; Department of Neuroradiology, King Fahad Medical City, Altakassusi Alliance Medical, Riyadh, Saudi Arabia.<br /><searchLink fieldCode="AU" term="%22Alanazy+MH%22">Alanazy MH</searchLink>; Department of Medicine, King Saud University Medical City and College of Medicine, King Saud University, Riyadh, Saudi Arabia.<br /><searchLink fieldCode="AU" term="%22Albash+B%22">Albash B</searchLink>; Kuwait Medical Genetics Centre, Ghanima Alghanim Building, Al-Sabah Medical Area, Kuwait.<br /><searchLink fieldCode="AU" term="%22Alaqeel+A%22">Alaqeel A</searchLink>; Department of Paediatrics, Ahmadi Hospital, Kuwait Oil Company (KOC), Kuwait.<br /><searchLink fieldCode="AU" term="%22Almontashiri+NA%22">Almontashiri NA</searchLink>; Center for Genetics and Inherited Diseases (CGID) and Faculty of Applied Medical Science, Taibah University, Madinah, Saudi Arabia.<br /><searchLink fieldCode="AU" term="%22Jamjoom+D%22">Jamjoom D</searchLink>; Department of Radiology, King Saud University Medical City and College of Medicine, King Saud University, Riyadh, Saudi Arabia.<br /><searchLink fieldCode="AU" term="%22Bashiri+FA%22">Bashiri FA</searchLink>; Division of Neurology, Department of Pediatric, College of Medicine, King Saud University Medical City, King Saud University, Riyadh, Saudi Arabia.<br /><searchLink fieldCode="AU" term="%22Hamad+MH%22">Hamad MH</searchLink>; Division of Neurology, Department of Pediatric, College of Medicine, King Saud University Medical City, King Saud University, Riyadh, Saudi Arabia.<br /><searchLink fieldCode="AU" term="%22Ali+HH%22">Ali HH</searchLink>; Research Center, College of Medicine, King Saud University, Saudi Arabia.<br /><searchLink fieldCode="AU" term="%22Alwatidi+M%22">Alwatidi M</searchLink>; Research Center, College of Medicine, King Saud University, Saudi Arabia.<br /><searchLink fieldCode="AU" term="%22Alharbi+E%22">Alharbi E</searchLink>; Center for Genetics and Inherited Diseases (CGID) and Faculty of Applied Medical Science, Taibah University, Madinah, Saudi Arabia.<br /><searchLink fieldCode="AU" term="%22Omar+S%22">Omar S</searchLink>; Kuwait Medical Genetic Centre, Ministry of Health, Suliabikhat 80901, Kuwait.<br /><searchLink fieldCode="AU" term="%22Marafi+D%22">Marafi D</searchLink>; Kuwait Medical Genetic Centre, Ministry of Health, Suliabikhat 80901, Kuwait; Department of Pediatrics, College of Medicine, Kuwait University, PO Box 24923, Safat 13110, Kuwait; Department of Pediatrics, Adan Hospital, Ministry of Health, Hadiya 52700, Kuwait.<br /><searchLink fieldCode="AU" term="%22Alabdulrazzaq+F%22">Alabdulrazzaq F</searchLink>; Kuwait Institute for Medical Specialization, Suliabikhat, PO Box 1793, Safat 13018, Kuwait.<br /><searchLink fieldCode="AU" term="%22Arold+ST%22">Arold ST</searchLink>; KAUST Center of Excellence for Smart Health, Biological and Environmental Science and Engineering Division, King Abdullah University of Science and Technology (KAUST), Thuwal 23955-6900, Saudi Arabia.<br /><searchLink fieldCode="AU" term="%22McFarland+R%22">McFarland R</searchLink>; Mitochondrial Research Group, Translational and Clinical Research Institute, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, UK; NHS Highly Specialised Services for Rare Mitochondrial Disorders, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK.<br /><searchLink fieldCode="AU" term="%22W+Taylor+R%22">W Taylor R</searchLink>; Mitochondrial Research Group, Translational and Clinical Research Institute, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, UK; NHS Highly Specialised Services for Rare Mitochondrial Disorders, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK.
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Academic+Press%22">Academic Press </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>9805456 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1096-7206 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2210967192%22">10967192 </searchLink><i>NLM ISO Abbreviation: </i>Mol Genet Metab <i>Subsets: </i>MEDLINE
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              Text: 2026 Jun
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