Fatal outcome after heart surgery in PMM2-CDG due to a rare homozygous gene variant with double effects.
Mol Genet Metab Rep
; 25: 100673, 2020 Dec.
Article
em En
| MEDLINE
| ID: mdl-33209585
ABSTRACT
Variants in Phosphomannomutase 2 (PMM2) lead to PMM2-CDG, the most frequent congenital disorder of glycosylation (CDG). We here describe the disease course of a ten-month old patient who presented with the classical PMM2-CDG symptoms as cerebellar hypoplasia, retinitis pigmentosa, seizures, short stature, hepato- and splenomegaly, anaemia, recurrent vomiting and inverted mamillae. A severe form of tetralogy of Fallot was diagnosed and corrective surgery was performed at the age of 10â¯months. At the end of the cardiopulmonary bypass, a sudden oedematous reaction of the myocardium accompanied by biventricular pump failure was observed immediately after heparin antagonization with protamine sulfate. The patient died seven days after surgery, since myocardial function did not recover on ECMO support. We here describe the first patient carrying the homozygous variant g.18313Aâ¯>â¯T in the PMM2 gene (NG_009209.1) that either can lead to c.394Aâ¯>â¯T (p.I132F) or even loss of 100â¯bp due to exon 5 skipping (c.348_447del; p.G117Rfs*4) which is comparable to a null allele. Proliferation and doubling time of the patient's fibroblasts were affected. In addition, we show that the induction of cellular stress by elevating the cell culture temperature to 40⯰C led to a decrease of the patients' PMM2 transcript as well as PMM2 protein levels and subsequently to a significant loss of residual activity. We assume that metabolic stressful processes occurring after cardiac surgery led to the drop of the patient's PMM activity below a life-sustaining niveau which paved the way for the fatal outcome.
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MEDLINE
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En
Revista:
Mol Genet Metab Rep
Ano de publicação:
2020
Tipo de documento:
Article
País de afiliação:
Alemanha