eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | jervell and lange-nielsen syndrome |
| Comorbidity | C0018784|sensorineural deafness |
| Sentences | 2 |
| PubMedID- 20809527 | Two phenotypic variants have been described: i) the more common autosomal dominant romano-ward syndrome (romano, et al., 1963; ward, 1964), and ii) the less common autosomal recessive jervell and lange-nielsen syndrome, which is associated with sensorineural deafness (jervell and lange-nielsen, 1957). |
| PubMedID- 23392653 | Surprisingly, 11 of these patients (73%) presented without the sensorineural deafness associated with jervell and lange-nielsen syndrome. |
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