Document Detail

Hemifacial myohyperplasia: description of a new syndrome.
MedLine Citation:
PMID:  11746014     Owner:  NLM     Status:  MEDLINE    
Hemifacial hypertrophy is a rare condition characterized by unilateral enlargement of all tissues of the face. We describe three patients who exhibit hemifacial hyperplasia of the muscles of facial expression with no other organ system involvement. These three cases, in addition to six other cases identified in the literature, describe a unique constellation of characteristics that place these patients into a distinct syndrome. We suggest that the term "hemifacial myohyperplasia" be used to describe this specific and unique condition.
S Lee; R Sze; C Murakami; J Gruss; M Cunningham
Related Documents :
8379034 - Extraordinary urinary frequency syndrome.
23633784 - Amelogenesis imperfecta and localised aggressive periodontitis: a rare clinical entity.
24461954 - The use of systematic reviews in clinical trials and narrative reviews in dermatology: ...
23480044 - Replantation of avulsed primary incisors: a critical review of a controversial treatment.
2583714 - Early yaws, imported in the netherlands.
24484694 - Reviewer acknowledgement 2013.
Publication Detail:
Type:  Case Reports; Journal Article    
Journal Detail:
Title:  American journal of medical genetics     Volume:  103     ISSN:  0148-7299     ISO Abbreviation:  Am. J. Med. Genet.     Publication Date:  2001 Nov 
Date Detail:
Created Date:  2001-12-17     Completed Date:  2002-01-31     Revised Date:  2004-11-17    
Medline Journal Info:
Nlm Unique ID:  7708900     Medline TA:  Am J Med Genet     Country:  United States    
Other Details:
Languages:  eng     Pagination:  326-33     Citation Subset:  IM    
Copyright Information:
Copyright 2001 Wiley-Liss, Inc.
Department of Otolaryngology, University of Washington, 1959 Pacific Street NE, Seattle, WA 98159, USA.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Child, Preschool
Facial Asymmetry / pathology*,  radiography
Facial Muscles / pathology*,  radiography
Tomography, X-Ray Computed
Comment In:
Am J Med Genet A. 2003 Jan 1;116A(1):103-4   [PMID:  12476465 ]

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine

Previous Document:  Molecularly defined interstitial tandem duplication 6p case with mild manifestations.
Next Document:  Connexin 26 gene (GJB2) mutation modulates the severity of hearing loss associated with the 1555A-->...