Sensorineural deafness in a child with Prader–Willi Syndrome—A rare case report
Prader–Willi syndrome (PWS) is a genetic condition, predominantly of sporadic origin, associated with chromosomal abnormalities involving the long arm of chromosome 15, specifically the q11–13 region. Of note, the STRC gene, located on chromosome 15q15.3, is implicated in congenital sensorineural he...
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| Main Authors: | , , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Wolters Kluwer Medknow Publications
2025-05-01
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| Series: | Journal of Family Medicine and Primary Care |
| Subjects: | |
| Online Access: | https://journals.lww.com/10.4103/jfmpc.jfmpc_1867_24 |
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