Descriptor English: | Facial Hemiatrophy | ||||||
Descriptor Spanish: |
Hemiatrofia Facial
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Descriptor Portuguese: | Hemiatrofia Facial | ||||||
Descriptor French: | Hémiatrophie faciale | ||||||
Entry term(s): |
Atrophies, Hemifacial Atrophies, Progressive Hemifacial Atrophy, Hemifacial Atrophy, Progressive Hemifacial Atrophy, Romberg Hemi-Facial Disease, Parry-Romberg Disease, Romberg Disease, Romberg's Facial Hemiatrophies Facial Hemiatrophies, Progressive Facial Hemiatrophy of Romberg Facial Hemiatrophy, Progressive Hemi-Facial Atrophy, Romberg Hemiatrophies, Facial Hemiatrophies, Progressive Facial Hemiatrophy, Facial Hemiatrophy, Progressive Facial Hemifacial Atrophies Hemifacial Atrophy Hemifacial Atrophy, Progressive Parry Romberg Disease Parry Romberg Syndrome Parry-Romberg Disease Parry-Romberg Syndrome Progressive Facial Hemiatrophies Progressive Facial Hemiatrophy Progressive Hemifacial Atrophies Progressive Hemifacial Atrophy Romberg Disease Romberg Facial Hemiatrophy Romberg Hemi Facial Atrophy Romberg Hemi-Facial Atrophy Romberg's Disease Rombergs Disease Syndrome, Parry-Romberg |
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Tree number(s): |
C07.465.284 C07.465.299.375 C10.292.319.375 |
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RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D005150 | ||||||
Scope note: | 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. |
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Annotation: | do not confuse with FACIAL ASYMMETRY; note HEMIFACIAL MICROSOMIA see FACIAL ASYMMETRY |
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Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CN congenital CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
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Public MeSH Note: | for ROMBERG DISEASE see ROMBERG'S DISEASE 1963-97 |
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DeCS ID: | 5251 | ||||||
Unique ID: | D005150 | ||||||
Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
Date Established: | 1966/01/01 | ||||||
Date of Entry: | 1999/01/01 | ||||||
Revision Date: | 2015/06/22 |
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Facial Hemiatrophy
- Preferred
Concept UI |
M0008116 |
Scope note | 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. |
Preferred term | Facial Hemiatrophy |
Entry term(s) |
Atrophies, Hemifacial Atrophies, Progressive Hemifacial Atrophy, Hemifacial Atrophy, Progressive Hemifacial Atrophy, Romberg Hemi-Facial Disease, Parry-Romberg Disease, Romberg Disease, Romberg's Facial Hemiatrophies Facial Hemiatrophies, Progressive Facial Hemiatrophy of Romberg Facial Hemiatrophy, Progressive Hemi-Facial Atrophy, Romberg Hemiatrophies, Facial Hemiatrophies, Progressive Facial Hemiatrophy, Facial Hemiatrophy, Progressive Facial Hemifacial Atrophies Hemifacial Atrophy Hemifacial Atrophy, Progressive Parry Romberg Disease Parry Romberg Syndrome Parry-Romberg Disease Parry-Romberg Syndrome Progressive Facial Hemiatrophies Progressive Facial Hemiatrophy Progressive Hemifacial Atrophies Progressive Hemifacial Atrophy Romberg Disease Romberg Facial Hemiatrophy Romberg Hemi Facial Atrophy Romberg Hemi-Facial Atrophy Romberg's Disease Rombergs Disease Syndrome, Parry-Romberg |
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