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Escher-Hirt syndrome.
Kotzot, D; Schlegel, C; Wichmann, W; Schinzel, A.
Afiliación
  • Kotzot D; Institute of Medical Genetics, University of Zürich.
Clin Dysmorphol ; 6(4): 315-21, 1997 Oct.
Article en En | MEDLINE | ID: mdl-9354839
A mother and her two daughters are reported with bilateral conductive deafness due to incudo-stapedial abnormalities, and microtia with thickened ear lobes. This pattern of abnormal findings, transmitted with an autosomal dominant mode of inheritance, is characteristic of the Escher-Hirt syndrome. One of the daughters died from an additional cardiac malformation (VSD). Anomalies of the middle ear were demonstrated in the surviving patients by computed tomography. Differential diagnosis with other genetic syndromes associated with deafness, and possible therapeutic approaches are discussed.
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Sordera / Oído Límite: Adult / Child / Female / Humans / Newborn Idioma: En Revista: Clin Dysmorphol Asunto de la revista: TERATOLOGIA Año: 1997 Tipo del documento: Article Pais de publicación: Reino Unido
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Sordera / Oído Límite: Adult / Child / Female / Humans / Newborn Idioma: En Revista: Clin Dysmorphol Asunto de la revista: TERATOLOGIA Año: 1997 Tipo del documento: Article Pais de publicación: Reino Unido