Disease: Congenital generalized fibromatosis
- A case of advanced infantile myofibromatosis harboring a novel MYH10-RET fusion
- A case report of infantile myofibromatosis of left mandibular angle
- A large mediastinal tumour invading into the liver with foetal hydrops: A rare case of infantile myofibromatosis
- A patient with germ-line gain-of-function PDGFRB p.N666H mutation and marked clinical response to imatinib
- A Rare Case of Infantile Myofibromatosis Presenting to the Emergency Department as Undiagnosed Long Bone Fractures
- A recurrent PDGFRB mutation causes familial infantile myofibromatosis
- A SAMD5-SASH1 fusion in solitary infantile myofibromatosis
- A tyrosine kinase-activating variant Asn666Ser in PDGFRB causes a progeria-like condition in the severe end of Penttinen syndrome
- Activating variants in PDGFRB result in a spectrum of disorders responsive to imatinib monotherapy
- Ambras syndrome: A rare case report
- An unusual cause of duodenal obstruction: mesenteric fibromatosis in a patient with type I Mayer-Rokitansky-Kuster-Hauser syndrome
- Atypical presentation of infantile digital fibromatosis
- Beyond infections: tumors and malformations of the diaper area
- Case report: rapid and durable response to PDGFR targeted therapy in a child with refractory multiple infantile myofibromatosis and a heterozygous germline mutation of the PDGFRB gene
- CD34-positive infantile myofibromatosis: Case report and review of hemangiopericytoma-like pattern tumors
- Chemotherapy for Generalized Infantile Myofibromatosis With Visceral Involvement
- Clinical and genetic evaluations of Zimmermann-Laband syndrome with gingival fibromatosis: a rare case report
- Congenital Generalized Hypertrichosis, Gingival Hyperplasia, a Coarse Facies with Constriction Bands: A Rare Association
- Congenital infantile myofibroma causing intrauterine death in a twin
- Congenital peribronchial myofibroblastic tumour with features of maturation in the older infant: report of two cases with a literature review
- Congenital peripheral ameloblastic fibroma with intraosseous involvement in a 2-week-old infant: A case report with review of literature
- De Novo 17q24.2-q24.3 microdeletion presenting with generalized hypertrichosis terminalis, gingival fibromatous hyperplasia, and distinctive facial features
- Desmoid tumor of Meckel's diverticulum presenting as intestinal obstruction: A rare case report with literature review
- Ectopic thyroid gland: clinical features and diagnostics in children
- Effects of Sunitinib and Other Kinase Inhibitors on Cells Harboring a <em>PDGFRB</em> Mutation Associated with Infantile Myofibromatosis
- Enhanced Collagen Deposition in the Duodenum of Patients with Hyaline Fibromatosis Syndrome and Protein Losing Enteropathy
- Epilepsy in KCNH1-related syndromes
- Exome sequencing identifies a novel homozygous variant in NDRG4 in a family with infantile myofibromatosis
- Expansion of the phenotype of Kosaki overgrowth syndrome
- Factors influencing and long-term effects of manual myotomy phenomenon during physiotherapy for congenital muscular torticollis
- Firm digital papulonodules in a young boy
- Generalized infantile myofibromatosis with a monophasic primitive pattern
- Generalized Infantile Myofibromatosis with Extensive Small Bowel Involvement in a Neonate
- Genetic architecture and phenotypic landscape of deafness and onychodystrophy syndromes
- Genetic testing for hereditary hyperparathyroidism and familial hypocalciuric hypercalcaemia in a large UK cohort
- Genomic analysis reveals germline and somatic PDGFRB variants with clinical implications in familial infantile myofibromatosis
- Giant stone in enterocystoplasty
- Gingival fibromatosis with congenital hypertrichosis
- Gingival fibromatosis with hypertrichosis syndrome: Case series of rare syndrome
- Gynecology and Oncology Fetal Myofibromatosis: A Challenge for Prenatal Diagnosis Mini Review of the English Literature
- Hereditary familial polyposis and Gardner's syndrome: contribution of the odonto-stomatology examination in its diagnosis and a case description
- Heterotopic ileal pancreas with lipoma and coexisting fibromatosis associated with a rare case of gastrointestinal bleeding. A case report and review of the literature
- Heterozygous PDGFRB Mutation in a Three-generation Family with Autosomal Dominant Infantile Myofibromatosis
- Infantile myofibroma: a firm, round plaque in an infant
- Infantile myofibromatosis
- Infantile myofibromatosis
- Infantile myofibromatosis - a clinical and pathological diagnostic challenge
- Infantile myofibromatosis as an unusual cause for unilateral atelectasis in an infant
- Infantile myofibromatosis in a 5-month-old boy
- Infantile Myofibromatosis of the Femoral Neck: A Case Report
- Infantile myofibromatosis of uterus: A case report
- Infantile Myofibromatosis With Cutaneous, Visceral, and CNS Involvement: A Multimodal Approach to Therapy
- Infantile Myofibromatosis With Intracranial Extradural Involvement and PDGFRB Mutation: A Case Report and Review of the Literature
- Infantile myofibromatosis: a series of 28 cases
- Infantile myofibromatosis: Excellent prognosis but also rare fatal progressive disease. Treatment results of five Cooperative Weichteilsarkom Studiengruppe (CWS) trials and one registry
- Infantile myofibromatosis: multiple firm nodules in a premature newborn
- Infantile myofibromatosis: review of imaging findings and emphasis on correlation between MRI and histopathological findings
- Infantile myofibromatosis. Study of a case using whole body ultrasound and MRI
- Intralesional 5-Fluorouracil: A Therapy for Solitary Infantile Myofibromatosis
- Intraspinal lesions associated with sacrococcygeal dimples
- Kidney transplantation in infantile myofibromatosis and fibromuscular dysplasia: a case report
- Major response to imatinib and chemotherapy in a newborn patient prenatally diagnosed with generalized infantile myofibromatosis
- Massive infantile myofibromatosis of the upper lip causing airway distress in a newborn
- Medical and surgical management of primary cardiac tumours in infants and children
- Modulation of expressivity in PDGFRB-related infantile myofibromatosis: a role for PTPRG?
- Morbidity after elective resection of prenatally diagnosed asymptomatic congenital pulmonary airway malformations
- Morphologic Overlap between Infantile Myofibromatosis and Infantile Fibrosarcoma: A Pitfall in Diagnosis
- Multicentric infantile myofibromatosis with extensive involvement limited to bone
- Multicentric myofibromatosis presenting as a large congenital eyelid myofibroma
- Multiple congenital malformations including generalized hypertrichosis with gum hypertrophy in a child exposed to valproic acid in utero
- Multiple firm erythematous nodules on the scalp of a child
- Multiple skin nodules in a newborn
- Mutations in PDGFRB cause autosomal-dominant infantile myofibromatosis
- Myofibromatosis presenting as reticulated vascular changes and subcutaneous atrophy in a patient with somatic mosaicism of PDGFRB mutation
- Nail Whispers Revealing Dermatological and Systemic Secrets: An Analysis of Nail Disorders Associated With Diverse Dermatological and Systemic Conditions
- Nonepithelial Tumors and Tumor-like Lesions of the Skin and Subcutis in Children
- Novel <em>PDGFRB</em> rearrangement in multifocal infantile myofibromatosis is tumorigenic and sensitive to imatinib
- Novel Oncogenic <em>PDGFRB</em> Variant in Severe Infantile Myofibromatosis With Response to Imatinib Using Therapeutic Drug Monitoring
- Partial trisomy of 11q23.3-q25 inherited from a maternal low-level mosaic unbalanced translocation
- PDGFRB gain-of-function mutations in sporadic infantile myofibromatosis
- PDGFRB mutants found in patients with familial infantile myofibromatosis or overgrowth syndrome are oncogenic and sensitive to imatinib
- Pediatric myofibroma/myofibromatosis of the soft tissue and bone: a clinicopathological analysis of 28 cases
- Perinatal sonographic diagnosis of cardiac fibroma with MR imaging correlation
- Polychondritis relapsans--a case report
- Prenatal diagnosis of infantile myofibromatosis of the lung: a case report and review of the literature
- Prenatal genetic diagnosis of disseminated infantile myofibromatosis: a case report and literature review
- Prenatal sonography of multicentric infantile myofibromatosis: Case report and review of the literature
- Proptosis secondary to infantile myofibromatosis in a newborn: role of the ophthalmologist from diagnosis to treatment
- Ruptured Infantile Myofibroma of the Head Presenting in a Neonate: Case Report and Review of the Literature
- Spontaneous Regression of an Infantile Scalp Tumor. Infantile myofibromatosis
- Sternocleidomastoid size and upper trapezius muscle thickness in congenital torticollis patients: A retrospective observational study
- Surgical treatment of cardiac fibroma in a child with left ventricular noncompaction
- Surgical treatment of left ventricular fibroma accompanied with ventricular septal defect in an infant: a case report
- Syndromic gingival fibromatosis
- Terminal osseous dysplasia with pigmentary defects (TODPD): Follow-up of the first reported family, characterization of the radiological phenotype, and refinement of the linkage region
- The Master of Puppets: Pleiotropy of PDGFRB and its Relationship to Multiple Diseases
- The spectrum of infantile myofibromatosis includes both non-penetrance and adult recurrence
- Treatment of generalized infantile myofibromatosis with sorafenib and imatinib: A case report
- Ulcerated congenital tumor. Solitary infantile myofibromatosis
- Vincristine and Dactinomycin in Infantile Myofibromatosis With a Review of Treatment Options