About this condition

HMGB1-related brachyphalangy, polydactyly and tibial aplasia syndrome

This is information, not medical advice. A doctor or genetic counsellor is the right person for decisions.

What this means, in plain words

HMGB1-related brachyphalangy, polydactyly and tibial aplasia syndrome is a rare condition linked to the HMGB1 gene.

No two people with this condition are the same, and not everything on this page will apply to everyone.

You are not alone

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People you can contact

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Things you can do this week

Write down your questions and take them to your next appointment (ours are below).

Questions to bring to your doctor

Has a gene change been found, and is it the kind usually seen in HMGB1-related brachyphalangy, polydactyly and tibial aplasia syndrome?
Is there a treatment for this condition, or a study we could join?
Should we see a genetic counsellor about what this means for the rest of the family?

Questions for our appointment

About: HMGB1-related brachyphalangy, polydactyly and tibial aplasia syndrome

Has a gene change been found, and is it the kind usually seen in HMGB1-related brachyphalangy, polydactyly and tibial aplasia syndrome?
Is there a treatment for this condition, or a study we could join?
Should we see a genetic counsellor about what this means for the rest of the family?

This is information, not medical advice. Prepared with Phenotech, a rare-disease atlas. Sources: ClinicalTrials.gov (https://clinicaltrials.gov/search?cond=HMGB1-related%20brachyphalangy%2C%20polydactyly%20and%20tibial%20aplasia%20syndrome&aggFilters=status:rec%20not).

Studies looking for participants

Looking for studies… Search ClinicalTrials.gov yourself ↗

The detailed view: how it works in the body, related diseases and research ideas.