AIM: To present a case of subacute juvenile Sandhoff disease (SD), a rare neurodegenerative disorder occurring in 1 in 4,00,000.
BACKGROUND: SD is a rare neurodegenerative disorder grouped under GM2 gangliosidosis that results from a mutation in the HEXB gene, which encodes the β-subunit of β-hexosaminidase, leading to a deficiency of hexosaminidases A and B. It affects the metabolism of GM2 gangliosides, causing the enzyme to accumulate within lysosomes in visceral cells as well as the central nervous system (CNS). Depending on the age of onset, the disease presents in three different phenotypes: (1) acute infantile SD, with onset before 6 months; (2) subacute juvenile SD (SJSD), with onset at 2-5 years; and (3) late-onset SD, with onset in late teens or young adulthood.
CARE DESCRIPTION: A rare case of a 10-year-old female child presented with right lower tooth pain. She had attained developmental milestones normally until about age 4 but later exhibited regressive changes around 4.5-5 years of age. She became progressively slow and unsteady. Investigations, including magnetic resonance imaging (MRI) of the brain, whole-exome sequencing, and biochemical genetic testing, led to a diagnosis of SJSD.
CONCLUSION: Not much literature has been published to highlight how SJSD impacts daily life and function. However, the functional limitations resulting from neurodegeneration may adversely affect daily activities.
CLINICAL SIGNIFICANCE: SJSD needs multidisciplinary involvement, including a physiotherapist, speech therapist, and psychiatrist, to monitor the prognosis regularly, diagnose future manifestations requiring supportive care, and ensure adequate functioning and activity of daily living.
HOW TO CITE THIS ARTICLE: Kadam BD, Jampanapalli SR, Ranganathan R, et al. Subacute Juvenile Sandhoff Disease: A Progressive Neurodegenerative Disorder. Int J Clin Pediatr Dent 2025;18(3):317-320.
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