Case study identifies dual genetic diagnosis of dyschromatosis universalis hereditaria and sensorineural hearing loss in a child, emphasizing the role of consanguinity.
8-year-male child, born of a second- degree consanguineous marriage, a known case of moderate intellectual disability was referred from the paediatric outpatient department with complaints of bilateral hearing loss of insidious onset.
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L Prasanth (2025) studied this question.
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