Concept information
Preferred term
Facial Hemiatrophy
Type
-
mesh:Descriptor
Definition
- A syndrome characterized by slowly progressive unilateral atrophy of facial subcutaneous fat, muscle tissue, skin, cartilage, and bone. The condition typically progresses over a period of 2-10 years and then stabilizes.
Broader concept
Entry terms
- Facial Hemiatrophy of Romberg
- Hemifacial Atrophy
- Hemifacial Atrophy, Progressive
- Parry-Romberg Disease
- Parry-Romberg Syndrome
- Progressive Facial Hemiatrophy
- Progressive Hemifacial Atrophy
- Romberg Disease
- Romberg Hemi-Facial Atrophy
- Romberg's Disease
Allowable Qualifier(s)
- blood (Qualifier)
- cerebrospinal fluid (Qualifier)
- chemically induced (Qualifier)
- classification (Qualifier)
- complications (Qualifier)
- congenital (Qualifier)
- diagnosis (Qualifier)
- diagnostic imaging (Qualifier)
- diet therapy (Qualifier)
- drug therapy (Qualifier)
- economics (Qualifier)
- embryology (Qualifier)
- enzymology (Qualifier)
- epidemiology (Qualifier)
- ethnology (Qualifier)
- etiology (Qualifier)
- genetics (Qualifier)
- history (Qualifier)
- immunology (Qualifier)
- metabolism (Qualifier)
- microbiology (Qualifier)
- mortality (Qualifier)
- nursing (Qualifier)
- parasitology (Qualifier)
- pathology (Qualifier)
- physiopathology (Qualifier)
- prevention & control (Qualifier)
- psychology (Qualifier)
- radiotherapy (Qualifier)
- rehabilitation (Qualifier)
- surgery (Qualifier)
- therapy (Qualifier)
- urine (Qualifier)
- veterinary (Qualifier)
- virology (Qualifier)
In other languages
-
French
-
Atrophie hémifaciale
-
Atrophie hémifaciale de Romberg
-
Atrophie hémifaciale progressive
-
Hémiatrophie faciale de Romberg
-
Hémiatrophie faciale progressive
-
Maladie de Parry-Romberg
-
Maladie de Romberg
-
Syndrome de Parry-Romberg
URI
http://data.loterre.fr/ark:/67375/JVR-NHVZZV8Q-W
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