From Surf Wiki (app.surf) — the open knowledge base

Terminal osseous dysplasia with pigmentary defects

Field	Value
name	Terminal osseous dysplasia with pigmentary defects
image	X-linked dominant.svg
caption	This condition is inherited in an X-linked dominant manner.
field	Dermatology

Terminal osseous dysplasia with pigmentary defects is a cutaneous condition characterized by hyperpigmented, atrophic facial macules.

It has been associated with FLNA.

References

Rapini, Ronald P.. (2007). "Dermatology: 2-Volume Set". Mosby.
(July 2010). "Terminal osseous dysplasia is caused by a single recurrent mutation in the FLNA gene". Am. J. Hum. Genet..

Info: Wikipedia Source

This article was imported from Wikipedia and is available under the Creative Commons Attribution-ShareAlike 4.0 License. Content has been adapted to SurfDoc format. Original contributors can be found on the article history page.

genodermatoses

Want to explore this topic further?

Ask Mako anything about Terminal osseous dysplasia with pigmentary defects — get instant answers, deeper analysis, and related topics.

Research with Mako

Free with your Surf account

Content sourced from Wikipedia, available under CC BY-SA 4.0.

This content may have been generated or modified by AI. CloudSurf Software LLC is not responsible for the accuracy, completeness, or reliability of AI-generated content. Always verify important information from primary sources.

Report