Isolated neurological presentations of mevalonate kinase deficiency

Eva M.M. Hoytema van Konijnenburg*, Esmeralda Oussoren, Joost Frenkel, Peter M. van Hasselt

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

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Abstract

Mevalonate kinase (MK) deficiency is a rare autosomal recessive metabolic disorder caused by pathogenic variants in the MVK gene with a broad phenotypic spectrum including autoinflammation, developmental delay and ataxia. Typically, neurological symptoms are considered to be part of the severe end of the phenotypical spectrum and are reported to be in addition to the autoinflammatory symptoms. Here, we describe a patient with MK deficiency with severe neurological symptoms but without autoinflammation and we found several similar patients in the literature. Possibly, the non-inflammatory phenotype is related to a specific genotype: the MVK p.(His20Pro)/p.(Ala334Thr) variant. There is probably an underdetection of the neurological MK deficient phenotype without inflammatory symptoms as clinicians may not test for MK deficiency when patients present with only neurological symptoms. In conclusion, although rare, neurological symptoms without hyperinflammation might be more common than expected in MK deficiency. It seems relevant to consider MK deficiency in patients with psychomotor delay and ataxia, even if there are no inflammatory symptoms.

Original languageEnglish
Pages (from-to)53-56
Number of pages4
JournalJIMD Reports
Volume64
Issue number1
Early online date18 Nov 2022
DOIs
Publication statusPublished - Jan 2023

Bibliographical note

Publisher Copyright:
© 2022 The Authors. JIMD Reports published by John Wiley & Sons Ltd on behalf of SSIEM.

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