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Last Updated: 10/31/2025
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Found 453 publications
Infantile myofibromatosis and capillary malformation of the skin due to PDGFRB mosaicism.
Journal: Molecular and cellular pediatrics
Published: April 30, 2025
Non-operative management of an infantile myofibroma in the palm.
Journal: The Journal of hand surgery, European volume
Published: March 27, 2025
Solitary infantile myofibromatosis presenting as multiple subcutaneous lesions: a case report.
Journal: Journal of medical case reports
Published: February 28, 2025
Infantile myofibromatosis: Small bumps pose big problems.
Journal: Journal of neonatal-perinatal medicine
Published: February 20, 2025
Treatment of PDGFRB-Related Penttinen Syndrome With Imatinib in a Young Child.
Journal: American journal of medical genetics. Part C, Seminars in medical genetics
Published: February 06, 2025
Multicentric infantile myofibromatosis with extensive visceral involvement in a newborn: case report.
Journal: Italian journal of pediatrics
Published: December 17, 2024
Novel PDGFRB Gene Fusions in Two Cases of Infantile Myofibromatosis.
Journal: Genes, chromosomes & cancer
Published: December 17, 2024
Variable response of germline activating PDGFRB variants to receptor tyrosine kinase inhibitors: implications for treatment.
Journal: European journal of human genetics : EJHG
Published: December 10, 2024
Infantile myofibromatosis of the forearm: A case report and literature review.
Journal: Radiology case reports
Published: November 22, 2024
A germline PDGFRB splice site variant associated with infantile myofibromatosis and resistance to imatinib.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: June 11, 2024
Late Relapse in Genetically Determined Infantile Myofibromatosis. A Case Report and Brief Focus on Recurrences.
Journal: Journal of pediatric hematology/oncology
Published: May 27, 2024
Last Updated: 10/31/2025