2020
DOI: 10.1002/jmd2.12165
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Fatal COVID‐19 infection in a patient with long‐chain 3‐hydroxyacyl‐CoA dehydrogenase deficiency: A case report

Abstract: Long‐chain fatty‐acyl CoA dehydrogenase deficiency (LCHADD) is an inborn error of long chain fatty acid oxidation with various features including hypoketotic hypoglycemia, recurrent rhabdomyolysis, pigmentary retinopathy, peripheral neuropathy, cardiomyopathy, and arrhythmias. Various stresses trigger metabolic decompensation. Coronavirus disease 2019 (COVID‐19) is a pandemic caused by the RNA virus SARS‐CoV‐2 with diverse presentations ranging from respiratory symptoms to myocarditis. We report a case of a pa… Show more

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Cited by 10 publications
(14 citation statements)
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References 32 publications
(43 reference statements)
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“…Most of the hospitalized patients were adults (16/22) with intoxication disorders (MMA, PA, and ASA) and 8 of those patients, in addition to a patient with Very long-chain Acyl-CoA dehydrogenase deficiency (VLCADD), developed severe symptoms and required intensive care management. This echoes the same course of previously reported IMD patients under these two categories ( Sibulo et al, 2021 ; Saad-Naguib et al, 2021 ; Kaur et al, 2021 ; Caciotti et al, 2020 ; Wongkittichote et al, 2020 ). Metabolic acidosis was mainly reported in patients with organic acidemias, while hyperammonemia was seen in ASA and PA patients.…”
Section: Discussionsupporting
confidence: 91%
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“…Most of the hospitalized patients were adults (16/22) with intoxication disorders (MMA, PA, and ASA) and 8 of those patients, in addition to a patient with Very long-chain Acyl-CoA dehydrogenase deficiency (VLCADD), developed severe symptoms and required intensive care management. This echoes the same course of previously reported IMD patients under these two categories ( Sibulo et al, 2021 ; Saad-Naguib et al, 2021 ; Kaur et al, 2021 ; Caciotti et al, 2020 ; Wongkittichote et al, 2020 ). Metabolic acidosis was mainly reported in patients with organic acidemias, while hyperammonemia was seen in ASA and PA patients.…”
Section: Discussionsupporting
confidence: 91%
“…Death due to complicated cardiomyopathy and heart failure during COVID-19 infection was reported in an infant with MPS-I ( Climent et al, 2020 ). Another reports of death were in a patient with Long-chain fatty-acyl CoA dehydrogenase deficiency due to COVID-19 complications and in another patient with Niemann-Pick C from complicated COVID-19 pneumonia and respiratory failure ( Wongkittichote et al, 2020 ; Tobór-Świętek et al, 2021 ). None of our patients with energy metabolism disorders died though, two of them developed rhabdomyolysis crisis during their COVID-19 illness.…”
Section: Discussionmentioning
confidence: 99%
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“…The grey literature search located no additional sources. Altogether, the evidence in this review includes 117 case reports/series 57 , 58 , 59 , 60 , 61 , 62 , 63 , 64 , 65 , 66 , 67 , 68 , 69 , 70 , 71 , 72 , 73 , 74 , 75 , 76 , 77 , 78 , 79 , 80 , 81 , 82 , 83 , 84 , 85 , 86 , 87 , 88 , 89 , 90 , 91 , 92 , 93 , 94 , 95 , 96 , 28 observational studies 10 , 11 , 139 , 140 , 141 , 142 , 143 , 144 , 145 , 146 , 147 , 148 , 149 , 150 , 151 , 152 , 153 , 154 , 155 , 156 , 157 , 158 , 159 , 160 , 161 , 162 , 163...…”
Section: Resultsmentioning
confidence: 99%
“…Interestingly, one study showed that mutations in the HADHA gene should be considered as a risk factor for a severe outcome of COVID-19. The patient, described in a single case report, with pathogenic variants in HADHA, suddenly developed acute respiratory failure due to COVID-19 infection, accompanied by refractory hypotension from severe cardiomyopathy which led to multiple organ failure and death [ 19 ].…”
Section: Discussionmentioning
confidence: 99%