Cardio-auditory syndromes. Cardiac and genetic study of 511 deaf-mute children.

Cascos, A Sánchez; Sánchez‐Harguindey, Luis; Rábago, P

doi:10.1136/hrt.31.1.26

Cited by 25 publications

(2 citation statements)

References 15 publications

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“…In the present material, only a few of the syndromes associated with inherited deafness (Konigsmark 1969) were found. ECG was not routinely performed, so cases of cardio-auditory syndromes (James 1967, Sanchez Cascos et al 1969, van Bruggen et al 1969, may have been overlooked. Two patients in the present material were considered possible examples of the fetal rubella syndrome because they were found to have cardiac abnormalities (Dahl and Boesen 1968).…”

Section: Discussionmentioning

confidence: 99%

School‐children with Perceptive Deafness

Gamstorp¹

1971

Develop Med Child Neuro

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SUMMARY This paper attempts to establish the cause of impaired hearing and the incidence of other defects in 112 children (49 girls, 63 boys) who were attending a special school for the hard of hearing. Information was obtained from a general physical and neurological examination, and where possible from a personal interview with the parents and from hospital records. Possible causes of deafness were hereditary factors, rubella during pregnancy, perinatal complications and meningitis. Other significant findings, including eye abnormalities, are discussed. RÉSUMÉ Enfants d'âge scolaire avec surdite de perception L'étude s'efforce d'établir la cause d'une insuffisance d'audition et l'incidence d'autres anomalies chez 112 enfants (49 fllles, 63 garçons) fréquentant une école spéciale pour sourds. Les informations ont été obtenues à partir d'examen physique général et neurologique ainsi que lorsque c'était possible, à partir d'une entrevue personnelle avec les parents ou encore à partir de dossiers hospitaliers. Les causes possibles des surditéétaient des facteurs héréditaires, une rougeole durant la grossesse, des complications péri‐natales ou des méningites. D'autres découvertes intéressantes comprenant des anomalies oculaires sont discutées. ZUSAMMENFASSUNG Schulkinder mit perceptiver Taubheit Diese Arbeit versucht, die Ursache der Schwerhörigkeit und die Häuflgkeit anderer Defekte bei 112 Kindern (49 Mädchen, 63 Knaben) zu ermitteln, die eine Spezialschule für schwerhörige Kinder besuchten. Die Informationen wurden durch eine allgemeine medizinische und neurologische Untersuchung gewonnen sowie, wenn möglich, durch eine persönliche Unterhaltung mit den Eltern und aus den Unterlagen von Krankenhäusern. Mögliche Ursachen der Taubheit waren erbliche Faktoren, Röteln während der Schwangerschaft, perinatale Komplikationen und Meningitis. Andere signiflkant Befunde, einschließlich Augenkrankheiten, werden diskutiert. RESUMEN Escolares con sordera de percepción Este trabajo trata de establecer la causa de una audición alterada y la incidencia de otros defectos en 112 niños (49 hembras y 63 varones) que asistian a un centro especial para los defectuosos del oído. Se obtuvo information de un examen general físico y neurológico y, cuando ello fue posible, por medio de una entrevista personal con los padres y de los datos obtenidos del hospital. Las posibles causas de sordera fueron factores hereditarios, rubeola durante la gestatión, complicaciones perinatales y meningitis. Se discuten otros hallazgos significativos, incluy‐endo anomalías oculares.

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Section: Discussionmentioning

confidence: 99%

School‐children with Perceptive Deafness

Gamstorp¹

1971

Develop Med Child Neuro

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“…Other inherited disorders of heart rate and myocardial conduction were described later (Romano et al 1963, Barlow et al 1964, Gamstorp et al 1964, Ward 1964, Garza et al 1970, Johansson & Jorming 1972. Arrhythmia in association with congenital deafness was also reported (Jervell & Lange-Nelson 1957, Levine & Woodworth 1958, Fraser et al 1964, Jervell et al 1966, James 1967, Sanchez Cascos et al 1969.…”

Section: Received 12 March Revised 12 May Accepted F O R Publicatiomentioning

confidence: 95%

Cardio‐cutaneous syndrome (the “LEOPARD” syndrome). Review of the literature and a new family

Seuánez

Mane-Garzon²,

Kolski

1976

Clinical Genetics

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Numerous reports of familial cardiac disorders associated with abnormalities of cutaneous pigmentation have appeared in the literature. In some of these there have been other somatic malformations including retardation of growth and anomalous development of the genitalia. In this paper we review the literature and describe another family with multiple lentigines occurring in six members out of eight examined. They were reported to occur in 10 other members not seen by us. The trait showed an autosomal dominant mode of inheritance and appeared to be transmitted by affected fathers. In previous reports transmission has usually been through an affected mother. In five of the six patients examined, only skin abnormalities were detected, but in the propositus the lentigines were associated with retardation of growth, hypertelorism, abnormal genitalia and complete atrioventricular block. The possible explanations for the lack of pleomorphy in other members of the family are discussed.

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Familial Q-T Prolongation Syndrome

Singer¹

1974

Arch Neurol

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Cardio-auditory syndromes. Cardiac and genetic study of 511 deaf-mute children.

Cited by 25 publications

References 15 publications

School‐children with Perceptive Deafness

School‐children with Perceptive Deafness

Cardio‐cutaneous syndrome (the “LEOPARD” syndrome). Review of the literature and a new family

Familial Q-T Prolongation Syndrome

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