Hereditary acrokeratotic poikiloderma

Get in touch with RARE Concierge.

Contact RARE Concierge

Hereditary acrokeratotic poikiloderma

Synonyms: Weary syndrome

A rare hereditary poikiloderma characterized by infantile onset of vesicopustule formation on hands and feet and widespread eczematoid dermatitis (both spontaneously resolving during childhood) as well as gradually developing diffuse poikiloderma with striate and reticulate atrophy (excluding the face scalp and ears) and development of keratotic papules on hands feet elbows and knees beginning in early childhood. There have been no further descriptions in the literature since 1981.

Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview.

Reference: Access aggregated data from Orphanet at Orphadata.

Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http://www.orphadata.org. Data version April 2024

Newly diagnosed with
Hereditary acrokeratotic poikiloderma?

Our RARE Concierge Services Guides are available to assist you by providing information, resources and connections as you navigate your rare disease journey.

Get Concierge Help

Advocacy Organizations

Clinical Trials

For a list of clinical trials in this disease area, please click here.