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RAB23-related Carpenter syndrome

MONDO:0008710

Any Carpenter syndrome in which the cause of the disease is a mutation in the RAB23 gene.

Also known as: ACPS 2, Carpenter syndrome, acrocephalopolysyndactyly type 2, Carpenter syndrome 1, Carpenter syndrome caused by mutation in RAB23, Carpenter syndrome type 1, RAB23 Carpenter syndrome, RAB23-related Carpenter syndrome

2 clinical trials for this condition and its sub-types, 0 tagged with RAB23-related Carpenter syndrome itself.

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Where it sits in the disease tree

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↑ Carpenter syndrome (0)

Including sub-types (2) Tagged with RAB23-related Carpenter syndrome (0)

Trials to join now! 1 Completed 1

Nano-ink gel could replace repeated skull surgeries for kids with rare genetic disorders

Disease control Recruiting now

This early-stage study aims to develop a personalized treatment for children with syndromic craniosynostosis, a group of rare genetic disorders where skull bones fuse too early. The approach uses a nano-engineered gel to deliver custom genetic medicine directly to the affected ar…

Sponsor: Fondazione Policlinico Universitario Agostino Gemelli IRCCS • Aim: Disease control

Last updated Sep 10, 2026 00:00 UTC

RAB23-related Carpenter syndrome

Where it sits in the disease tree

Nano-ink gel could replace repeated skull surgeries for kids with rare genetic disorders