Parry-Romberg syndrome
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| Parry-Romberg syndrome Classification and external resources | |
| ICD-10 | G51.8 |
|---|---|
| ICD-9 | 349.89 |
| OMIM | 141300 |
| DiseasesDB | 30151 |
| MeSH | D005150 |
Parry-Romberg syndrome (sometimes called just Romberg syndrome) is a rare, incurable craniofacial disorder which is characterized by the slow atrophy of the subcutaneous (under the skin) muscle usually on half of the face (hemifacial atrophy). It has a higher prevalence in females and normally appears between the ages of 5 and 15. The condition also causes neurological symptoms, including seizures and severe facial pain.[1]
It is classed as a rare disease in the United States.
Eponym
The name comes from Parry (1825) and Henoch and Romberg (1846) who first described the disease.[1][1]
References
Acknowledgement and Attribution Regarding Sources of Content
Some of the initial content on this page may be incorporated in part from copyleft sources in the public domain including wikis such as Wikipedia and AskDrWiki. Drug information for patients came from the The National Library of Medicine. Infectious disease information may have come from the Centers for Disease Control (CDC). Differential Diagnoses are drawn from clinicians as well as an amalgamation of 3 sources: 1.The Disease Database; 2. Kahan, Scott, Smith, Ellen G. In A Page: Signs and Symptoms. Malden, Massachusetts: Blackwell Publishing, 2004:3; 3. Sailer, Christian, Wasner, Susanne. Differential Diagnosis Pocket. Hermosa Beach, CA: Borm Bruckmeir Publishing LLC, 2002:7 .
