Willard ("Bill") E. Fee, Jr.

Publication Details

  • CONRADI-HUNERMAN SYNDROME - CASE-REPORT ANNALS OF OTOLOGY RHINOLOGY AND LARYNGOLOGY Hochman, M., Fee, W. E. 1987; 96 (5): 565-568

    Abstract:

    Conradi-Hunerman syndrome, a variant of chondrodysplasia punctata, rarely presents with primary manifestations relevant to the head and neck surgeon. Usually, the disease is evidenced by malformation of the extremities, cataracts, cutaneous lesions, and an unusual facies. We have followed a child with Conradi-Hunerman syndrome for 7 years whose primary manifestation of the disease is respiratory compromise secondary to calcification of the laryngotracheobronchial tree. In addition, he has a conductive hearing loss thought to be secondary to ossicular chain fixation.

    View details for Web of Science ID A1987K570500017

    View details for PubMedID 3674654

Stanford Medicine Resources:

Footer Links: