Key result
Developmental delay represents the earliest and most prevalent symptom in 94% of cerebral Alexander disease cases.
Why the study?
The study was designed to determine the ages at acquisition of developmental milestones, loss of motor function, and clinical symptoms in Alexander disease.
Observational (n=51)
p-value: p=<.0001
The clinical triad of developmental delay, seizures, and macrocephaly are not universally present in cerebral Alexander disease, with developmental delay being the earliest and most prevalent symptom.
No takes yet. Share an insight, caveat, or question.
Developmental delay may prompt earlier evaluation for cerebral Alexander disease; extends phenotypic data but leaves diagnostic criteria open for validation.
Objective: To determine the ages at acquisition of developmental milestones, loss of motor function, and clinical symptoms in Alexander disease. Methods: Patients with confirmed cerebral Alexander disease were included. Data abstraction of developmental and disease-specific milestones was performed from medical records, physical exams, and questionnaires. Mixed effects logistic regression was used to determine if key clinical features were associated with milestone achievement, controlling for patient age. Results: 51 patients with cerebral/infantile Alexander disease were evaluated at a mean age of 10.96 years (range 2.29-31.08 years). Developmental milestones in Alexander disease were often achieved but delayed. Ambulation was achieved in 44 subjects (86%); 34 (67%) subjects walked independently (mean age 1.9 years, range 0.91-3.25 years) and an additional 10 (20%) subjects walked with assistance (mean age 3.9 years, range 1.8-8 years) but did not progress to independent ambulation. Developmental delay was the earliest and most prevalent symptom (N = 48 [94%], mean age 0.58 years), compared to an initial seizure (N = 41 [80%], mean age 2.80 years), and macrocephaly (N = 28 [55%], mean age 4.04 years), P < .0001 between these ages of onset. Loss of independent ambulation occurred in 11 of the 34 (32%) children who had acquired ambulation (range 3.41-15.10 years). Presence of seizures or macrocephaly did not predict the achievement or loss of ambulation. Conclusions: The clinical triad of developmental delay, seizures, and macrocephaly are not universally present in cerebral Alexander disease. Clinicians should have a high index of suspicion for Alexander disease in patients with mild delays and a first seizure.
Joung et al. (2023) conducted an observational in Cerebral Alexander disease (n=51). In cerebral Alexander disease, developmental delay was the earliest and most prevalent symptom (94%, mean age 0.58 years) compared to initial seizure (80%) and macrocephaly (55%) (P < .0001).
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: