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Recurrent hypocalcaemic seizures: diagnosing 22q11.2 deletion syndrome in early adulthood

Year: 2026

Type: article

Study design: Case Report

Source: BMJ Case Reports

DOI: 10.1136/bcr-2025-267427

Authors: Chaitra Kannadka, Arundhati Girish Diwan, Swati Chouhan, Bryan Koithara

Institution: Bharati Vidyapeeth (Deemed to be University)

Language: English

Topic: Genomic variations and chromosomal abnormalities

Subfield: Genetics

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

OpenAlex ID: W7122371249

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Cites: 9

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