LA SINDROME DI JERVELL E LANGE-NIELSEN. REVISIONE DELLA LETTERATURA CON APPROFONDIMENTO DI UN CASO

Translated title of the contribution: Jervell and Lange-Nielsen syndrome

U. Ambrosetti, A. Zaghis

Research output: Contribution to journalArticle

1 Citation (Scopus)

Abstract

Jervell and Lange-Nielsen (1975) first described a syndrome characterized by congenital nerve deafness, prolongation of the QT interval in the ECG, syncopal attacks and sudden death. An important difference between this syndrome and the syndrome described by Romano-Ward (episodes of unconsciousness, also sudden death in some cases and furthermore prolongation of QT) is the congenital deafness which is not found in the cases described by Romano-Ward. The cause of fainting and the reasons for the prolongation of the QT interval have been exhaustively discussed: no definite explanation has been found. The condition was supposed to be due to an inborn error of myocardial metabolism, caused by some unknown enzymatic deficiency. Abnormalities of the T waves themselves have also been observed and include large, bifid or inverted form. The long QT interval causes an abnormally long vulnerable period, enhancing the possibility that ectopic beats will trigger a ventricular dysrhythmia and attacks of syncope provoked by exertion or mental stress. The resemblance to attacks of angina pectoris is obvious but are certainly not caused by coronary ischemia. In treating syncopal attacks of this syndrome, several drugs should theoretically be of value: digitalis to shorten the QT interval, a beta-receptor blocking agent to reduce adrenergic hyperactivity, and a sedative to control emotional hyperreaction. Several Authors have discussed the genetic problems; they find a high frequency of consanguineous unions among the parents of affected children, and they conclude that the data are consistent with a hypothesis of recessive inheritance. Those heterozygous for the gene may have slight or moderate prolongation of the QT interval. Anaemia has been observed in many patients with this syndrome. This anaemia was hypochromic, microcytic, and other laboratory findings were also consistent with iron deficiency anaemia. The main clinical features shown by a case of Jervell and Lange-Nielsen syndrome are described in this paper.

Original languageItalian
Pages (from-to)253-261
Number of pages9
JournalOtorinolaringologia
Volume35
Issue number3
Publication statusPublished - 1985

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Jervell-Lange Nielsen Syndrome
Syncope
Deafness
Sudden Death
Romano-Ward Syndrome
Inborn Errors Metabolism
Unconsciousness
Iron-Deficiency Anemias
Digitalis
Angina Pectoris
Hypnotics and Sedatives
Adrenergic Agents
Anemia
Electrocardiography
Ischemia
Parents
Pharmaceutical Preparations
Genes

ASJC Scopus subject areas

  • Otorhinolaryngology

Cite this

LA SINDROME DI JERVELL E LANGE-NIELSEN. REVISIONE DELLA LETTERATURA CON APPROFONDIMENTO DI UN CASO. / Ambrosetti, U.; Zaghis, A.

In: Otorinolaringologia, Vol. 35, No. 3, 1985, p. 253-261.

Research output: Contribution to journalArticle

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