Aug 2026· Annals of Clinical and Translational Neurology· 0 citations· 38 references
Medicine
Abstract
ABSTRACT Objective The aim of this study was to characterize intellectual and motor function, neurological features including epilepsy, treatment response, and adaptive behavior in patients with pyruvate dehydrogenase complex deficiency (PDCD) in Sweden. Methods Forty‐two individuals with genetically confirmed PDCD (86% PDHA1‐related disease) were identified from a nationwide epidemiological study and were included in this cross‐sectional study comprising systematic neurological evaluations (n = 41) and caregiver interviews assessing adaptive behavior (n = 35). Results Intellectual disability was detected in 33/42 (79%) individuals, while 31/35 (89%) demonstrated significant impairments in adaptive functioning. Although 27/39 (69%) were ambulatory, only 8/39 (21%) demonstrated age‐appropriate walking ability. Clinical signs of polyneuropathy were observed in 24/41 (59%), bulbar symptoms in 22/41 (54%), spasticity in 19/41 (46%), ataxia in 13/41 (32%), and dystonia in 9/41 (22%). Lifetime epilepsy was present in 16/41 (39%) of individuals. Ketogenic diet treatment, administered to 30 individuals, was effective in both prenatal‐ and postnatal‐onset disease. Seizure frequency decreased in individuals with epilepsy (8/9; 89%) and relapses of dystonia, ataxia, exercise intolerance, and lactic acidosis were prevented in all affected individuals (15/15). Improvements in communication and motor function were also noted. Discussion Intellectual disability and deficits in adaptive behavior are frequent in PDCD, although cognitive outcomes are more heterogeneous among individuals with postnatal onset. Prenatal onset and epilepsy are associated with severe‐profound intellectual disability. Although most are ambulatory, motor deficits are frequent. A ketogenic diet treatment is a safe and effective therapeutic option, contributing to both seizure control and remission of neurological deterioration relapses.
IEM represent an important and potentially treatable cause of pediatric stroke, particularly in populations with high consanguinity, and recognition of characteristic clinical features, distinctive MRI patterns, and supportive EEG findings can facilitate early diagnosis.
J. Alvi, Areeba Wasim, Saher Gul Ahdi et al.· Frontiers in Neurology· 0 citations
The findings suggest a potential increased frequency of seizures in classic infantile Pompe disease in comparison with unaffected children, occurring predominantly after the age of 7, and that epilepsy is part of the CNS phenotype.
M. C. Faraguna, Alexander Broomfield, S. Gasperini et al.· Neurology: Genetics· 0 citations
The findings underscore the importance of incorporating cognitive evaluation and management into comprehensive epilepsy care, particularly in resource-limited settings where cognitive morbidity may be underrecognized.
S. Allen, C. Phillips, M. T. Wardle et al.· medRxiv· 0 citations
Improvements in group-level performance improved in six of the twenty tests administered, of which three remained significant after correction for multiple comparisons, while 28 of 42 patients (66.7%) still scored in the impaired range on at least one test at 12 months, and 17 (40.5%) on two or more.
Giulia Del Duca, M. Camici, Isabella Sperduti et al.· Neurology International· 0 citations
This study investigated long‐term cognitive development and genotype–phenotype relationships in patients with Mucopolysaccharidosis Type II (MPS II). A nationwide prospective cohort study was conducted in the Netherlands with cognitive follow‐up since 2007. Patients were classified as neuronopathic or non‐neuronopathic...
J. Holdorp, M. E. Michelle Kruijshaar, A. A. M. Audrey Vollebregt et al.· Journal of Inherited Metabol...· 0 citations
Abstract Objective Rett syndrome (RTT) is a severe neurodevelopmental disorder frequently associated with drug‐resistant epilepsy, autonomic dysfunction, respiratory abnormalities, sleep disturbances, and behavioral impairment. Fenfluramine has shown efficacy in developmental and epileptic encephalopathies and may prov...
E. González-Alguacil, Nuria Lamagrande Casanova, Manuel Luján-Bonete et al.· Epilepsia Open· 0 citations
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