CBL-related disorder

Disease Overview

CBL-related disorder is a genetic condition caused by pathogenic variants in the Cbl ubiquitin ligase gene, (CBL; HGNC:1541). Due to the proposed mechanism indicating the CBL gene’s relationship to the RAS-MAPK pathway and the phenotypic presentation similar to that of the RASopathies, CBL-related disorder should be considered a RASopathy disorder. Though there is a wide spectrum of phenotypic variability, broadly, patients with CBL-related disorder have presented with developmental delay, intellectual disability, neurodevelopmental alterations, prenatal lymphatic anomalies, cardiac malformations as well as vascular anomalies particularly affecting the brain (e.g. Moya-moya arteriopathies), craniofacial features indicative of a RASopathy, hypotonia, feeding difficulties, edema of the legs, musculoskeletal and respiratory thorax abnormalities, ectodermal features including cafe-au-lait spots, immunological and hematological disorders and susceptibility to tumors diagnosed as juvenile myelomonocytic leukemia (JMML) that is usually self-remitting. Note tumor risk beyond JMML has not yet been thoroughly assessed. Due to the clinical presentation of a broad spectrum of these and other phenotypes in patients with variants in CBL, these conditions are currently defined by experts in reference to the causal gene, CBL.

Synonyms

• CBL-related disorder
• Cbl mutation-associated syndrome
• Cbl syndrome
• NSLL
• Noonan syndrome-like disorder with JMML
• Noonan syndrome-like disorder with juvenile myelomonocytic leukaemia
• Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
• Noonan syndrome-like disorder with or without juvenile myelomonocytic leukaemia
• Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia
• Noonan-like syndrome