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Our rare endocrine tumour guidelines are intended to be a reference document for clinicians presented with the challenge of managing children and young people with rare endocrine tumour diagnoses.

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Join us in celebrating excellence at the 2025 CCLG & TYAC Annual Conference. Nominations are now OPEN for the CCLG & TYAC Member Awards!

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Sign up to the CCLG Abseil Adventure.

Rhabdomyosarcoma, a cancer that usually affects muscles, is the most common soft-tissue sarcoma in children. Overall, around 65% of children with rhabdomyosarcoma will survive, but the cure rates vary depending on different characteristics of the disease.