Otolaryngologic Findings in Whistling Face Syndrome
- 1 November 1989
- journal article
- research article
- Published by American Medical Association (AMA) in JAMA Otolaryngology–Head & Neck Surgery
- Vol. 115 (11) , 1373-1380
- https://doi.org/10.1001/archotol.1989.01860350107025
Abstract
• Craniocarpotarsal dysplasia or Whistling face syndrome is rare with only 60 cases having been reported in the literature. More than 60 anatomic anomalies of the head, hands, and feet, in addition to the face, have been noted. Although the literature contains numerous case reports describing in detail the various features and abnormalities of the syndrome, the otolaryngologic findings in these patients have yet to be summarized. We present two additional cases in a mother and daughter with an extended follow-up period of 30 and 17 years, respectively, and summarize the otolaryngologic findings in all previously reported cases of this rare syndrome. Also, the principal clinical features and associated features are described. (Arch Otolaryngol Head Neck Surg. 1989;115:1373-1380)This publication has 4 references indexed in Scilit:
- Further evidence for genetic heterogeneity of whistling face or Freeman‐Sheldon syndrome in a Chinese familyAmerican Journal of Medical Genetics, 1987
- Autosomal Recessive Type of Whistling Face Syndrome in TwinsPediatrics, 1982
- Recessive form of Freeman-Sheldon's syndrome or 'whistling face'.Journal of Medical Genetics, 1977
- Craniocarpotarsal dysplasia or whistling face syndromePlastic and Reconstructive Surgery, 1970