Bell’s palsy
Bell's palsy is a neurological disorder characterized by sudden, unilateral facial paralysis or weakness. This condition arises from dysfunction of the seventh cranial nerve, known…
Chronic phase philadelphia chromosome positive chronic myelocytic leukemia
Chronic myelocytic leukemia (CML) is a hematologic malignancy characterized by the presence of the Philadelphia chromosome (Ph+), which results from a reciprocal translocation between chromosomes…
Cytomegalovirus disease
Cytomegalovirus diseaseis a member of the Herpesviridae family and is a prevalent virus affecting individuals of all ages. While many infections remain asymptomatic, CMV poses…
Cytokine release syndrome
Cytokine Release Syndrome (CRS) is an acute systemic inflammatory response characterized by fever and multiple organ dysfunction, often triggered by infections or certain immunotherapies. It…
Cystinuria
Cystinuria is a rare inherited disorder that leads to the formation of recurrent kidney stones due to excessive excretion of cystine in the urine. This…
Cystic fibrosis with responsive cftr mutation
Cystic fibrosis (CF) is a life-threatening genetic disorder caused by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene. This gene is responsible for…
Cystic fibrosis with heterozygous f508del mutation in cftr gene
Cystic fibrosis (CF) is a genetic disorder characterized by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene. Among these mutations, the F508del variant…