Erythema palmaris hereditarium
General Information (adopted from Orphanet):
| Synonyms, Signs: |
Lane disease Red palms disease |
| Number of Symptoms | 3 |
| OrphanetNr: | 231031 |
| OMIM Id: |
133000
|
| ICD-10: |
L59.8 |
| UMLs: |
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| MeSH: |
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| MedDRA: |
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| Snomed: |
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Prevalence, inheritance and age of onset:
| Prevalence: | No data available. |
| Inheritance: |
Autosomal dominant [Orphanet] |
| Age of onset: |
Neonatal Infancy [Orphanet] |
Disease classification (adopted from Orphanet):
| Parent Diseases: |
Unclassified genetic skin disease
-Rare genetic disease -Rare skin disease |
Symptom Information:
|
|
(HPO:0010783) | Erythema | 138 / 7739 | ||||
|
|
(MedDRA:10033551) | Palmar erythema | 2 / 7739 | ||||
|
|
(HPO:0000006) | Autosomal dominant inheritance | 2518 / 7739 |
Associated genes:
ClinVar (via SNiPA)
| Gene symbol | Variation | Clinical significance | Reference |
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Additional Information:
| Description: (OMIM) |
Erythema palmare hereditarium is a benign condition that was first described by Lane (1929). Erythema usually presents at birth and remains stable throughout life. Histology shows dilated vessels in the entire dermis with inflammatory infiltrate. Capillaroscopy reveals an ... |
| Clinical Description OMIM |
Sarma and Wang (2007) described a 44-year-old Chinese man, his mother, and his 7-year-old daughter who had red hands since birth. The condition was asymptomatic. There was no hyperhidrosis, hyperkeratosis, or any scaling. No erythema was noted on ... |