Spondylocarpotarsal synostosis syndrome

MONDO:0010094

Spondylocarpotarsal synostosis (SCT) syndrome is a skeletal dysplasia clinically characterized by postnatal progressive vertebral fusions frequently manifesting as block vertebrae, contributing to an undersized trunk and a disproportionate short stature, scoliosis, lordosis, carpal and tarsal synostosis, with club feet and a mild facial dysmorphism.

Also known as: SCT, Synspondylism, spondylocarpotarsal syndrome, spondylocarpotarsal synostosis, spondylocarpotarsal synostosis syndrome, vertebral fusion with carpal coalition, Synspondylism congenital, Synspondylism, congenital

2 clinical trials for this condition and its sub-types, 2 tagged with Spondylocarpotarsal synostosis syndrome itself.

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Where it sits in the disease tree

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Part of

↑ Bone development disease (528) ↑ Filamin-related bone disorder (4) ↑ Spondylodysplastic dysplasia (2)

Including sub-types (2) Tagged with Spondylocarpotarsal synostosis syndrome (2)

Trials to join now! 1 Completed 1

Personalized mutation tracking could spot relapse sooner in bone marrow cancer patients

Knowledge-focused Completed

This study looked at 308 people with myelodysplastic syndromes (MDS) who had a stem cell transplant. Researchers identified each patient's unique genetic mutations and then monitored those mutations in blood and bone marrow samples after transplant. The goal was to see if rising …

Sponsor: Nordic MDS Group • Aim: Knowledge-focused

Last updated Jun 27, 2026 12:23 UTC

Spondylocarpotarsal synostosis syndrome

Where it sits in the disease tree

Personalized mutation tracking could spot relapse sooner in bone marrow cancer patients