Neonatal-onset multiple acyl-CoA dehydrogenase deficiency (MADD) in the ETFDH gene: A case report and a literature review. Issue 37 (11th September 2020)

• Record Type: Journal Article
• Authors: Ding, Meijuan; Liu, Ruihua; Qiubo, Li; Zhang, Yanke; Kong, Qingxia
• Other Names: Saranathan. Maya section editor.
• Is Part Of: Medicine. Volume 99:Issue 37(2020)
• Publication Date: 2020-09-11
• Subjects: ETFDH -- glutaric aciduria type II -- MADD -- review; Medicine -- Periodicals; Medicine -- Periodicals; Médecine -- Périodiques; Geneeskunde; Medicine; Periodicals; Periodicals; 610.5
• DOI: 10.1097/MD.0000000000021944
• Languages: English
• ISSNs: 0025-7974

Abstract

Abstract: Rationale: Multiple acyl-CoA dehydrogenase deficiency (MADD) is a rare inborn error of metabolism affecting fatty acid, amino acid, and choline metabolism. The clinical manifestation of MADD is heterogeneous, from severe neonatal forms to mild late-onset forms. Patient concerns: Here, we report a patient who presented with severe hypoglycemia and exercise intolerance suggestive of MADD. Serum tandem mass spectrometry analysis indicated elevated levels of various acyl carnitines at 25 days of age. Exome sequencing of the proband revealed compound heterozygous mutations, c. 413T>G (p.Leu138Arg) and c.1667C > G (p.Pro556Arg), in the ETFDH gene as the probable causative mutations. Diagnoses: Based on the patient's clinical presentation and test results, the patient was diagnosed with MADD. Interventions: A high-calorie and reduced-fat diet was given together with oral supplements of L-carnitine (150 mg/day). Outcomes: He passed away at the age of 4 months because of severe respiratory distress accompanied by muscle weakness. Lessons: He passed away at the age of 4 months because of severe respiratory distress accompanied by muscle weakness. Clinicians should consider MADD in the differential diagnosis when patients present with muscle weakness and biochemical abnormalities. Gene testing plays a critical role in confirming the diagnosis of MADD and may not only prevent the need for invasive testing but also allow for timely initiation of treatment.