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GTR Home > Conditions/Phenotypes > Acrodermatitis continua suppurativa of Hallopeau

Acrodermatitis continua suppurativa of Hallopeau

Synonyms
ACRODERMATITIS CONTINUA OF HALLOPEAU; INTERLEUKIN 36 RECEPTOR ANTAGONIST DEFICIENCY; Psoriasis 14, pustular
Modes of inheritance
Autosomal recessive inheritance (Orphanet)

Summary

A rare, genetic, chronic, recurrent, slowly progressive, epidermal disease characterized by small, sterile, pustular eruptions, involving the nails and surrounding skin of the fingers and/or toes, which coalesce and burst, leaving erythematous, atrophic skin where new pustules develop. Onychodystrophy is frequently associated and anonychia and osteolysis are reported in severe cases. Local expansion (to involve the hands, forearms and/or feet) and involvement of mucosal surfaces (e.g. conjunctiva, tongue, urethra) may be observed. [from ORDO]

Available tests

4 tests are in the database for this condition.

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Clinical tests (4 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: FIL1, FIL1(DELTA), FIL1D, IL-36Ra, IL1F5, IL1HY1, IL1L1, IL1RP3, IL36RA, PSORP, PSORS14, IL36RN
    Summary: interleukin 36 receptor antagonist

Clinical features

Help
Imported from Human Phenotype Ontology (HPO)

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