Seborrhea-like Dermatitis With Psoriasiform Elements

Description

Seborrhea-like dermatitis with psoriasiform elements is a rare, genetic, epidermal disorder characterized by a chronic, diffuse, fine, scaly erythematous rash on the face (predominantly the chin, nasolabial folds, eyebrows), around the earlobes and over the scalp, associated with hyperkeratosis over elbows, knees, palms, soles and metacarpophalangeal joints, in the absence of associated rheumatological or neurological disorders. Cold weather, emotional stress and strenuous physical activity may exacerbate symptoms.

Clinical Features

Phenotypes and symptoms related to Seborrhea-like Dermatitis With Psoriasiform Elements

  • Hyperkeratosis
  • Arthralgia
  • Arthritis
  • Skin rash
  • Overgrowth
  • Epidermal acanthosis
  • Inflammatory abnormality of the skin
  • Psoriasiform dermatitis
  • Parakeratosis
  • Seborrheic dermatitis

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.

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.

Seborrhea-like Dermatitis With Psoriasiform Elements Recommended genes panels

Panel Name, Specifity and genes Tested/covered
ZNF750.

By Fulgent Genetics Fulgent Genetics (United States).

ZNF750
Specificity
100 %
Genes
100 %
Tempus xT assay.

By Tempus Labs, Inc. (United States).

BCL6, RIT1, BCL7A, BCR, ROS1, RPL5, RPS15, RPS6KB1, RUNX1, RXRA, BLM, SDHA, SDHB, SDHC, SDHD, SEC23B, SEMA3C, BMPR1A, SF3B1, SRSF2 , (...)

View the complete list with 555 more genes
Specificity
1 %
Genes
100 %
Tempus xO assay.

By Tempus Labs, Inc. (United States).

BCL6, RHEB, RIPK1, RIPK2, RIPK3, RIT1, BCL7A, BCL9, BCR, ROBO2, ROCK1, ROCK2, ROR1, ROR2, ROS1, RPA1, BDNF, RPL5, RPN1, RPS6KB1 , (...)

View the complete list with 1627 more genes
Specificity
1 %
Genes
100 %

You can get up to -5 more panels with our dedicated tool

Learn more

Sources and references

You can check the following sources for additional information.

MESH OMIM ORPHANET Genetic Syndrome Finder

If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like CHILBLAIN LUPUS 2; CHBL2 CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2S; CMT2S DENYS-DRASH SYNDROME; DDS CHROMOSOME Xq27.3-q28 DUPLICATION SYNDROME ARTHROGRYPOSIS-LIKE SYNDROME AMYOTROPHIC LATERAL SCLEROSIS 1; ALS1 MCCUNE-ALBRIGHT SYNDROME; MAS