A clinical case of myelodysplastic syndrome with monosomy 7 in a patient with a mutation in the SAMD9L gene
Conditions associated with defects in the SAMD9 and SAMD9L genes are a group of nosologies with a range of clinical symptoms from multisystem lesions in the framework of MIRAGE syndrome to isolated hematological manifestations. The article presents a clinical case of a patient with myelodysplastic syndrome and a...