Mitochondrial disorder associated with newborn cardiopulmonary arrest

Kyunglim L. Yoon, Susan G. Ernst, Cynthia Rasmussen, Elizabeth C. Dooling, June R. Aprille

Research output: Contribution to journalArticlepeer-review

29 Scopus citations

Abstract

A female infant who died 2.5 d after birth with hypoglycemia, lactic acidosis, and sudden multisystem failure was studied. Biochemical studies showed complex HI and IV deficiency in liver, kidney, and muscle, with muscle most severely affected. Southern blot analysis of the patient’s mitochondrial DNA did not reveal any deletions. Denaturing gradient gel analysis, which detects single base changes by differences in melting behavior, showed an extra band that was not seen in mitochondrial DNA from the mother, the mother’s identical twin sister, or an unrelated normal subject. This extra band indicated heteroplasmy for a restriction fragment containing the apocytochrome b and transfer RNAthr genes. Sequencing revealed an A to G mutation at nucleotide 15923, the last 1 base of the anticodon loop of the transfer RNAthr gene. The mutation lengthens the anticodon stem by added pairing and reduces the anticodon loop size from 7 to 5 nucleotides, potentially compromising transfer RNAthr function in translation and/or in processing the polycistronic RNA; transcript. The patient’s mother previously had a male 1 infant who also died at 1.5 d postnatal, and both the mother 1 and her twin have had multiple miscarriages. Amniocentesis for a genetic screen was performed on the mother’s; twin sister during a recent pregnancy; some of the cultured cells were made available for this study. The mutation was not found in the amniocytes or in umbilical cord blood obtained at birth; the baby was normal at birth and remains healthy. It is concluded that the mutation at nucleotide 15923 was most likely the cause of the fatal disease in the index case. The timing of the illness was consistent with postnatal depletion of glycogen reserves. The findings suggest that a mitochondrial disorder should be considered for infants who experience sudden cardiopulmonary arrest within the first few days of life.

Original languageEnglish
Pages (from-to)433-440
Number of pages8
JournalPediatric Research
Volume33
Issue number5
DOIs
StatePublished - May 1993

Fingerprint

Dive into the research topics of 'Mitochondrial disorder associated with newborn cardiopulmonary arrest'. Together they form a unique fingerprint.

Cite this