Jeune syndrome - GRK2-related

MONDO:0100583

A form of Jeune syndrome caused by biallelic loss-of-function variants in the GRK2 gene.

Also known as: GRK2-related Jeune syndrome, asphyxiating thoracic dystrophy - GRK2-related, short rib polydactyly - GRK2 related, short rib thoracic dystrophy - GRK2 related

1 clinical trial for this condition and its sub-types, 0 tagged with Jeune syndrome - GRK2-related itself.

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↑ Jeune syndrome (2)

Including sub-types (1) Tagged with Jeune syndrome - GRK2-related (0)

Trials to join now! 1

Could a diabetes drug protect kidneys in children with genetic disease?

Disease control Recruiting now

This study tests whether adding dapagliflozin (a diabetes drug) to standard care reduces protein leakage in the urine of children with hereditary kidney diseases. About 44 children will receive either dapagliflozin plus standard care or standard care alone for 12 weeks, then swit…

Phase 3 • Sponsor: Children's Hospital of Fudan University • Aim: Disease control

Last updated Jul 08, 2026 00:00 UTC

Jeune syndrome - GRK2-related

Where it sits in the disease tree

Could a diabetes drug protect kidneys in children with genetic disease?