Full Mouth Rehabilitation of a Child with Aicardia-Goutières: A Rare Syndrome

Pathak, Pradnya Dileep and Shah, Preetam P and Lakade, Laxmi S and Shinde, Maya U (2023) Full Mouth Rehabilitation of a Child with Aicardia-Goutières: A Rare Syndrome. JOURNAL OF CLINICAL AND DIAGNOSTIC RESEARCH, 17 (1). ZD19-ZD21. ISSN 2249782X

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Abstract

Aicardi-Goutières Syndrome (AGS) is a rare genetic disorder with autosomal recessive inheritance. AGS is characterised by an early-onset encephalopathy that usually, but not always, results in severe intellectual and physical disability. Involuntary muscular spasms between the ages of four months and four years are the typical starting point for Aicardi syndrome. Hepatosplenomegaly, increased liver enzymes, thrombocytopenia, and abnormal neurologic signs in a subgroup of AGS children at birth strongly imply congenital infection. Agenesis of the corpus callosum, chorioretinal lacunae, and seizures are all symptoms of Aicardi syndrome. They frequently exhibit the subacute onset of a severe encephalopathy that is characterised by intense irritability, sporadic sterile pyrexias, loss of abilities, and slowed head growth. In 40% of cases, skin lesions like chilblains can appear on the fingers, toes, and ears. This disease can be diagnosed with Magnetic Resonance Imaging (MRI) and Computed Tomography (CT) scans with the appearance of calcification of the basal ganglia. The associated behavioural challenges with syndromic patients demand pharmacological management of oral rehabilitation. The literature is scarce regarding the oral manifestations of this syndrome. Hence, authors present the successful full-mouth rehabilitation of severe Early Childhood Caries (ECC) in a 3-year-old child with AGS under General Anaesthesia (GA).

Item Type: Article
Subjects: Journal Eprints > Medical Science
Depositing User: Managing Editor
Date Deposited: 14 Jun 2023 03:26
Last Modified: 16 Jan 2024 04:54
URI: http://repository.journal4submission.com/id/eprint/2271

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