Escher Hirt Syndrome

Overview

Type of disease: Rare conditions

Escher-Hirt syndrome is characterized by small ears with thickened ear lobes, a small jaw, and conductive hearing loss due to ear abnormalities. It has only been described in a few families. Escher-Hirt syndrome is inherited in an autosomal dominant pattern. Source: Genetic and Rare Diseases Information Center (GARD), supported by ORDR-NCATS and NHGRI.

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