Lelis syndrome
Source: Wikipedia, the free encyclopedia.
Medical condition
| Lelis syndrome | |
|---|---|
| Other names | Ectodermal dysplasia-acanthosis nigricans syndrome |
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| This condition is inherited in an autosomal recessive manner. | |
| Specialty | Medical genetics |
Lelis syndrome is a genetic disorder, a rare condition with
See also
- List of cutaneous conditions
References
External links
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AR | ||
XR | ||
| Ungrouped |
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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 |
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|---|---|
| Other |
anomalies
| Midline |
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|---|---|
| Nevus |
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| Other/ungrouped |
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