A De Novo HECW2 Variant in a Patient with Acetazolamide-Responsive Episodic Ataxia
© 2022. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature..
To the best of our knowledge, this is the first case to address episodic ataxia (EA) as a possible phenotypic feature of HECW2-related disorder. This single case study describes a 26-year-old female born at term with mild intellectual disability, neonatal hypotonia, and a history of febrile seizures who presented with paroxysmal events since the age of 2. These episodes include frequent falls due to imbalance, dilated pupils, vertigo, diaphoresis, nausea, vomiting, and nystagmus. Brain imaging was normal. A prolonged electroencephalogram (EEG) revealed interictal epileptiform discharges but failed to capture her clinical events. For several years, she was treated for presumed focal seizures with preserved awareness and trialed on adequate dosing of several antiepileptic medications without improvement. After 25 years, given the more prolonged nature of her episodes and the mild interictal cerebellar signs, empiric treatment with acetazolamide was initiated for a presumed diagnosis of EA. Acetazolamide treatment led to a dramatic reduction in event frequency and severity. The initial EA genetic panel was negative. Clinical exome sequence analysis revealed a novel pathogenic de novo missense variant in the HECW2 gene [c.3829 T > C;(p.Tyr1277His)], located in the HECT domain. HECW2 variants are associated with neurodevelopmental delay, hypotonia, and epilepsy. This study expands the genetic and clinical spectrum of HECW2-related disorder and adds EA to the phenotypic spectrum in affected individuals.
Medienart: |
E-Artikel |
---|
Erscheinungsjahr: |
2023 |
---|---|
Erschienen: |
2023 |
Enthalten in: |
Zur Gesamtaufnahme - volume:22 |
---|---|
Enthalten in: |
Cerebellum (London, England) - 22(2023), 5 vom: 20. Okt., Seite 1029-1033 |
Sprache: |
Englisch |
---|
Beteiligte Personen: |
Tedesco Silva, Leticia Maria [VerfasserIn] |
---|
Links: |
---|
Themen: |
Acetazolamide |
---|
Anmerkungen: |
Date Completed 08.09.2023 Date Revised 22.09.2023 published: Print-Electronic Citation Status MEDLINE |
---|
doi: |
10.1007/s12311-022-01458-5 |
---|
funding: |
|
---|---|
Förderinstitution / Projekttitel: |
|
PPN (Katalog-ID): |
NLM345064887 |
---|
LEADER | 01000naa a22002652 4500 | ||
---|---|---|---|
001 | NLM345064887 | ||
003 | DE-627 | ||
005 | 20231226024226.0 | ||
007 | cr uuu---uuuuu | ||
008 | 231226s2023 xx |||||o 00| ||eng c | ||
024 | 7 | |a 10.1007/s12311-022-01458-5 |2 doi | |
028 | 5 | 2 | |a pubmed24n1150.xml |
035 | |a (DE-627)NLM345064887 | ||
035 | |a (NLM)35987951 | ||
040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
041 | |a eng | ||
100 | 1 | |a Tedesco Silva, Leticia Maria |e verfasserin |4 aut | |
245 | 1 | 2 | |a A De Novo HECW2 Variant in a Patient with Acetazolamide-Responsive Episodic Ataxia |
264 | 1 | |c 2023 | |
336 | |a Text |b txt |2 rdacontent | ||
337 | |a ƒaComputermedien |b c |2 rdamedia | ||
338 | |a ƒa Online-Ressource |b cr |2 rdacarrier | ||
500 | |a Date Completed 08.09.2023 | ||
500 | |a Date Revised 22.09.2023 | ||
500 | |a published: Print-Electronic | ||
500 | |a Citation Status MEDLINE | ||
520 | |a © 2022. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature. | ||
520 | |a To the best of our knowledge, this is the first case to address episodic ataxia (EA) as a possible phenotypic feature of HECW2-related disorder. This single case study describes a 26-year-old female born at term with mild intellectual disability, neonatal hypotonia, and a history of febrile seizures who presented with paroxysmal events since the age of 2. These episodes include frequent falls due to imbalance, dilated pupils, vertigo, diaphoresis, nausea, vomiting, and nystagmus. Brain imaging was normal. A prolonged electroencephalogram (EEG) revealed interictal epileptiform discharges but failed to capture her clinical events. For several years, she was treated for presumed focal seizures with preserved awareness and trialed on adequate dosing of several antiepileptic medications without improvement. After 25 years, given the more prolonged nature of her episodes and the mild interictal cerebellar signs, empiric treatment with acetazolamide was initiated for a presumed diagnosis of EA. Acetazolamide treatment led to a dramatic reduction in event frequency and severity. The initial EA genetic panel was negative. Clinical exome sequence analysis revealed a novel pathogenic de novo missense variant in the HECW2 gene [c.3829 T > C;(p.Tyr1277His)], located in the HECT domain. HECW2 variants are associated with neurodevelopmental delay, hypotonia, and epilepsy. This study expands the genetic and clinical spectrum of HECW2-related disorder and adds EA to the phenotypic spectrum in affected individuals | ||
650 | 4 | |a Case Reports | |
650 | 4 | |a Journal Article | |
650 | 4 | |a Adult | |
650 | 4 | |a Epilepsy | |
650 | 4 | |a Episodic ataxia | |
650 | 4 | |a HECW2 | |
650 | 7 | |a Acetazolamide |2 NLM | |
650 | 7 | |a O3FX965V0I |2 NLM | |
650 | 7 | |a Anticonvulsants |2 NLM | |
650 | 7 | |a HECW2 protein, human |2 NLM | |
650 | 7 | |a EC 2.3.2.26 |2 NLM | |
650 | 7 | |a Ubiquitin-Protein Ligases |2 NLM | |
650 | 7 | |a EC 2.3.2.27 |2 NLM | |
700 | 1 | |a Sharma, Sonali |e verfasserin |4 aut | |
700 | 1 | |a Schrauwen, Isabelle |e verfasserin |4 aut | |
700 | 1 | |a Margolesky, Jason |e verfasserin |4 aut | |
700 | 1 | |a Detyniecki, Kamil |e verfasserin |4 aut | |
773 | 0 | 8 | |i Enthalten in |t Cerebellum (London, England) |d 2002 |g 22(2023), 5 vom: 20. Okt., Seite 1029-1033 |w (DE-627)NLM126368899 |x 1473-4230 |7 nnns |
773 | 1 | 8 | |g volume:22 |g year:2023 |g number:5 |g day:20 |g month:10 |g pages:1029-1033 |
856 | 4 | 0 | |u http://dx.doi.org/10.1007/s12311-022-01458-5 |3 Volltext |
912 | |a GBV_USEFLAG_A | ||
912 | |a GBV_NLM | ||
951 | |a AR | ||
952 | |d 22 |j 2023 |e 5 |b 20 |c 10 |h 1029-1033 |