Drummond Fever Syndrome is a relatively rare genetic disorder in which the main symptoms in infants include peculiar facial features, abnormal development of multiple organs and limb deformities. Consult the relevant doctor for examination. 1. Specialized facial features: Specialized facial features are often used in clinical diagnosis, such as arched eyebrows, abnormal eye lashes, ear deformities and long human body. In severe cases, it may also lead to facial atrophy. 2. Abnormal development of multiple organs: Abnormal development of multiple organs, such as the heart, may lead to ventricular septal defect or atrial septal defect; abnormal development of the brain may lead to mental retardation. 3. Limb deformities: infants are prone to missing bones, leading to limb deformities. For example, if the bones of the hand are missing, the fingers will be missing, and in serious cases, the limbs will be mutilated. If an infant has any of the above symptoms, it is recommended to consult a doctor in time to clarify the cause of the disease and actively cooperate with the doctor for treatment.