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B063 Jervell and Lange-Nielsen Syndrome

✍ Scribed by A. Eftekharian; N. Alani


Book ID
117339196
Publisher
Elsevier Science
Year
2011
Tongue
English
Weight
37 KB
Volume
75
Category
Article
ISSN
0165-5876

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Jervell and Lange-Nielsen syndrome (MIM 220400; JLNS), is a rare form of profound congenital deafness combined with syncopal attacks and sudden death due to prolonged QTc; it is an autosomal recessive trait. After its first description in Norway in 1957, later reports from many other countries have