Dyschromatosis universalis hereditaria
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Medical condition
| Dyschromatosis universalis hereditaria | |
|---|---|
| Specialty | Dermatology |
Dyschromatosis universalis hereditaria is a type of
spots formed like lace in a generalized distribution.[1]
Both
recessive inheritance have been reported with the disorder.[2]
It has been associated with mutations in genes SASH1 and ABCB6.[citation needed]
It is a rare genodermatosis.[1]
References
- ^ ISBN 978-0-323-54753-6.
- S2CID 9623609.
External links
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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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