Steatocystoma multiplex: Difference between revisions
Jump to navigation
Jump to search
m (Robot: Automated text replacement (-{{SIB}} +, -{{EH}} +, -{{EJ}} +, -{{Editor Help}} +, -{{Editor Join}} +)) |
m (Robot: Automated text replacement (-{{reflist}} +{{reflist|2}}, -<references /> +{{reflist|2}}, -{{WikiDoc Cardiology Network Infobox}} +)) |
||
| Line 24: | Line 24: | ||
==References== | ==References== | ||
{{reflist}} | {{reflist|2}} | ||
==External links== | ==External links== | ||
Revision as of 15:05, 6 September 2012
| Steatocystoma multiplex | |
| ICD-10 | L72.2 |
|---|---|
| ICD-9 | 706.2 |
| OMIM | 184500 |
| DiseasesDB | 29808 |
| eMedicine | derm/404 |
Steatocystoma multiplex is a congenital condition resulting in multiple cysts on the body.
Causes
It is associated with defects in Keratin 17.[1]
Treatment
The cysts can be moved via excision, though conventional cyst excision techniques have proven impractical, and a specialized regimen is required.[2]
References
- ↑ Smith FJ, Corden LD, Rugg EL; et al. (1997). "Missense mutations in keratin 17 cause either pachyonychia congenita type 2 or a phenotype resembling steatocystoma multiplex". J. Invest. Dermatol. 108 (2): 220–3. PMID 9008238.
- ↑ Pamoukian VN, Westreich M (1997). "Five generations with steatocystoma multiplex congenita: a treatment regimen". Plast. Reconstr. Surg. 99 (4): 1142–6. PMID 9091916.