Save information for later
Sign Up

Learn About Hemifacial Hyperplasia Strabismus

What is the definition of Hemifacial Hyperplasia Strabismus?
Bencze syndrome or hemifacial hyperplasia with strabismus is a malformation syndrome involving the abnormal growth of the facial skeleton as well as its soft tissue structure and organs, and is characterized by mild facial asymmetry with unaffected neurocranium and eyeballs, as well as by esotropia, amblyopia and/or convergent strabismus, and occasionally submucous cleft palate. Transmission is autosomal dominant. There have been no further descriptions in the literature since 1979.
What are the alternative names for Hemifacial Hyperplasia Strabismus?
  • Hemifacial hyperplasia strabismus
  • Bencze syndrome
Who are the top Hemifacial Hyperplasia Strabismus Local Doctors?
Otolaryngology | Allergy and Immunology
Otolaryngology | Allergy and Immunology

Marshall Medical Center

4300 Golden Ctr Dr, Suite D, 
Placerville, CA 
 (85.2 mi)
Languages Spoken:
English

Robert Chase is an Otolaryngologist and an Allergy and Immunologist in Placerville, California. Dr. Chase and is rated as an Advanced provider by MediFind in the treatment of Hemifacial Hyperplasia Strabismus. His top areas of expertise are Burning Mouth Syndrome, Glossodynia, Infant Hearing Loss, Perichondritis, and Laryngectomy.

Providence Medical Foundation

3307 Renner Dr, 
Fortuna, CA 
 (206.9 mi)
Languages Spoken:
English

Gregory Barkdull is an Otolaryngologist in Fortuna, California. Dr. Barkdull and is rated as an Experienced provider by MediFind in the treatment of Hemifacial Hyperplasia Strabismus. His top areas of expertise are Tonsil Stones, Acinic Cell Carcinoma of Salivary Glands, Salivary Gland Tumors, Adenoid Cystic Carcinoma, and Myringotomy.

 
 
 
 
Learn about our expert tiers
Learn More
What are the latest Hemifacial Hyperplasia Strabismus Clinical Trials?
Match to trials
Find the right clinical trials for you in under a minute
Get started
Who are the sources who wrote this article ?

Published Date: May 02, 2022
Published By: Genetic and Rare Diseases Informnation Center