Atrophoderma Vermiculata
Description
Atrophoderma vermiculata, a form of keratosis pilaris atrophicans, typically presents in childhood with erythema and follicular keratotic papules that slowly progress to characteristic atrophy, which has been described as worm-eaten, reticular, or honeycomb, and occurs on the cheeks, preauricular area, and forehead. More rarely, the atrophy may extend to the upper lip, helices, ear lobes, and, in some cases, the limbs. The degree of inflammation, the presence of milia, and the extent of follicular plugs are variable (summary by Luria and Conologue, 2009).
Clinical Features
Top most frequent phenotypes and symptoms related to Atrophoderma Vermiculata
- Edema
- Dilatation
- Alopecia
- Hyperkeratosis
- Erythema
- Scarring
- Skin rash
- Papule
- Falls
- Abnormality of the cardiovascular system
And another 11 symptoms. If you need more information about this disease we can help you.
Incidence and onset information
— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)— No data available about the known clinical features onset.
Alternative names
Atrophoderma Vermiculata Is also known as atrophodermia reticulata symmetrica faciei, folliculitis ulerythematosa reticulate, honeycomb atrophy, folliculitis ulerythematosa reticulata, atrophodermia vermiculata.
Researches and researchers
Currently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.Atrophoderma Vermiculata Recommended genes panels
| Panel Name, Specifity and genes Tested/covered |
|---|
 NOONAN, LEOPARD, COSTELLO and CARDIOFACIOCUTANEOUS SYNDROME.
By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases (Spain).
RIT1, SHOX, BRAF, SOS1, SPRY2, SRC, CD2AP, GAB2, CBL, SHOC2, SRCAP, SPRED1, ANKRD11, CRK, CRKL, EGFR, ERBB2, FGFR3, AKT1, HRAS , (...)
View the complete list with 24 more genes
Specificity
3 %
Genes
100 % |
 LRP1.
By Fulgent Genetics Fulgent Genetics (United States).
LRP1
Specificity
100 %
Genes
100 % |
You can get up to -6 more panels with our dedicated tool
Learn moreSources and references
You can check the following sources for additional information.
ORPHANET OMIM Rare Disease Search EngineIf you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like ISOLATED PIERRE ROBIN SYNDROME IMMUNODEFICIENCY 31B; IMD31B HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 7; HHF7