Telangiectasia macularis eruptiva perstans
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Human disease
Medical condition
| Telangiectasia macularis eruptiva perstans | |
|---|---|
| Specialty | Medical genetics  |
Telangiectasia macularis eruptiva perstans is persistent, pigmented, asymptomatic eruption of macules usually less than 0.5 cm in diameter with a slightly reddish-brown tinge.[1]: 616 [2]
See also
- Mastocytosis
- Skin lesion
- List of cutaneous conditions
References
- ISBN 0-7216-2921-0.
- ISBN 978-1-4160-2999-1.
External links
| Classification | ILDS Q82.296) |
|---|
| ||
|---|---|---|
AR | ||
XR | ||
| Ungrouped |
| |
and related
- EBS
- EBS-K
- EBS-WC
- EBS-DM
- EBS-OG
- EBS-MD
- EBS-MP
- JEB
- JEB-H
- Mitis
- Generalized atrophic
- JEB-PA
- DEB
- DDEB
- RDEB
- related: Costello syndrome
- Kindler syndrome
- Laryngoonychocutaneous syndrome
- Skin fragility syndrome
- Naegeli syndrome/Dermatopathia pigmentosa reticularis
- Hay–Wells syndrome
- Hypohidrotic ectodermal dysplasia
- Focal dermal hypoplasia
- Ellis–van Creveld syndrome
- Rapp–Hodgkin syndrome/Hay–Wells syndrome
keratinopathy
| PPK |
|
|---|---|
| Other |
anomalies
| Midline |
|
|---|---|
| Nevus |
|
| Other/ungrouped |
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