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Atrophoderma vermiculata

Disease definition

A rare genetic skin disease characterized by childhood onset of follicular keratotic papules slowly progressing to characteristic ''honeycomb'' atrophy on the cheeks, preauricular area, and forehead. Less frequently, the condition may affect also the upper lip, ears, or limbs. Additional features include facial erythema, milia, and follicular plugs.

ORPHA:79100

Classification level: Disorder
  • Synonym(s):
    • Folliculitis ulerythematosa reticulate
  • Prevalence: Unknown
  • Inheritance: Unknown or Autosomal recessive 
  • Age of onset: Childhood
  • ICD-10: L66.4
  • ICD-11: ED56
  • OMIM: 209700  604093
  • UMLS: C0263429
  • MeSH: -
  • GARD: 9744
  • MedDRA: -

  A summary on this disease is available in Español (2020) Français (2020) Nederlands (2020)

Additional information

Further information on this disease

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Specialised Social Services

The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.