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Baller-Gerold syndrome

MONDO:0009039

Baller-Gerold syndrome is characterized by the association of coronal craniosynostosis with radial ray anomalies (oligodactyly, aplasia or hypoplasia of the thumb, aplasia or hypoplasia of the radius).

Also known as: Baller-Gerold syndrome, BALLER-Gerold syndrome, BGS, craniosynostosis with radial defects, craniosynostosis-radial aplasia syndrome

1 clinical trial for this condition and its sub-types.

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Broader categories

Disease (680) Musculoskeletal system disorder (207) Hereditary disease (176) Bone disorder (51) Syndromic disease (25) Craniosynostosis (15) Human disease (14) Skeletal system disorder (4) Bone development disease (2) Disease of genetic or genomic mechanism (2)
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  • Nano-ink gel could replace repeated skull surgeries for kids with rare genetic disorders

    Disease control Not yet recruiting

    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 Jun 27, 2026 12:09 UTC

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