Kasabach-Merritt Syndrome

Kasabach Merritt syndrome (KMS) is a rare progressive disease with foci of venous invasion leading to thrombosis, hemorrhage, and infections.

*Causes*

The commonality of the causes of CMS and other malignant neoplasms, together with the detection of a viral oncogene in CMS cells, makes it possible to assume a high probability of detecting the viral nature of tumors in

Kasabach Merritt syndrome is a rare syndrome **Kasabach and Merritt syndrome** is a group of hereditary syndromes of vascular nevus syndrome (oncology), which includes characteristic symptoms: the formation of multiple moles on the skin from red to brown, fibroangitic tissue, purple vascular formations, lymphocytic infiltration of the skin.

Description of the disease This rare disease occurs due to damage to the "SOS2" gene on chromosome 7. The disruption of normal cell growth is caused by DNA damage or the proliferation of abnormal cells. By this