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Sökning: (WFRF:(Brunner Han G.)) srt2:(2020-2023) > An E280K Missense V...

An E280K Missense Variant in KCND3/Kv4.3—Case Report and Functional Characterization

Ågren, Richard (författare)
Department of Physiology and Pharmacology, Karolinska Institutet, Stockholm, Sweden
Geerdink, Niels (författare)
Department of Pediatrics, Rijnstate Hospital, Arnhem, Netherlands
Brunner, Han G. (författare)
Department of Human Genetics, Donders Centre for Brain, Cognition and Behavior, Radboud University Medical Center, Nijmegen, Netherlands; Department of Clinical Genetics, MUMC Maastricht, GROW School for Oncology and Developmental Biology, MHENS School for Mental Health and Neuroscience, Maastricht University Medical Center, Maastricht, Netherlands
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Paucar, Martin (författare)
Department of Neurology, Karolinska University Hospital, Stockholm, Sweden; Department of Clinical Neuroscience, Karolinska Institutet, Stockholm, Sweden
Kamsteeg, Erik-Jan (författare)
Department of Human Genetics, Radboud UMC, Nijmegen, Netherlands
Sahlholm, Kristoffer (författare)
Umeå universitet,Institutionen för integrativ medicinsk biologi (IMB),Wallenberg centrum för molekylär medicin vid Umeå universitet (WCMM),Department of Physiology and Pharmacology, Karolinska Institutet, Stockholm, Sweden
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 (creator_code:org_t)
MDPI, 2023
2023
Engelska.
Ingår i: International Journal of Molecular Sciences. - : MDPI. - 1661-6596 .- 1422-0067. ; 24:13
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • A five-year-old girl presented with headache attacks, clumsiness, and a history of transient gait disturbances. She and her father, mother, twin sister, and brother underwent neurological evaluation, neuroimaging, and exome sequencing covering 357 genes associated with movement disorders. Sequencing revealed the new variant KCND3 c.838G>A, p.E280K in the father and sisters, but not in the mother and brother. KCND3 encodes voltage-gated potassium channel D3 (Kv4.3) and mutations have been associated with spinocerebellar ataxia type 19/22 (SCA19/22) and cardiac arrhythmias. SCA19/22 is characterized by ataxia, Parkinsonism, peripheral neuropathy, and sometimes, intellectual disability. Neuroimaging, EEG, and ECG were unremarkable. Mild developmental delay with impaired fluid reasoning was observed in both sisters, but not in the brother. None of the family members demonstrated ataxia or parkinsonism. In Xenopus oocyte electrophysiology experiments, E280K was associated with a rightward shift in the Kv4.3 voltage-activation relationship of 11 mV for WT/E280K and +17 mV for E280K/E280K relative to WT/WT. Steady-state inactivation was similarly right-shifted. Maximal peak current amplitudes were similar for WT/WT, WT/E280K, and E280K/E280K. Our data indicate that Kv4.3 E280K affects channel activation and inactivation and is associated with developmental delay. However, E280K appears to be relatively benign considering it does not result in overt ataxia.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinsk bioteknologi -- Medicinsk bioteknologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Medical Biotechnology -- Medical Biotechnology (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Neurovetenskaper (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Neurosciences (hsv//eng)

Nyckelord

electrophysiology
episodic ataxia
mild developmental delay
rare variants
spinocerebellar ataxia type 19/22
voltage sensor
voltage-gated potassium channel D3

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