There are more types of associated X chromosome recessive genetic diseases, the more common ones are hemophilia, progressive muscular dystrophy, albinism and so on. 1. Hemophilia: It is a hereditary coagulation dysfunction disease, characterized by bleeding, including joint bleeding, soft tissue bleeding, muscle hematoma and so on. If it is acute bleeding period, coagulation factors should be injected as soon as possible to stop bleeding, such as vitamin K, and then combined with aminomethylsulfonic acid, aminocaproic acid treatment, the use of drugs should be in accordance with the doctor’s prescription. 2. Progressive muscular dystrophy: It is an extremely rare genetic defective disease, which is mainly characterized by skeletal muscle weakness and will cause muscle atrophy when the condition worsens. After diagnosis, glucocorticosteroids, such as prednisone and prednisone, should be used as soon as possible according to medical advice. 3. Albinism: mainly due to genetic mutations leading to abnormalities in melanin production, which can easily cause skin cancer if not treated in time. It should be kept away from ultraviolet rays during treatment, and bone marrow transplantation can be considered when there are serious defects. In addition to the above, X chromosome recessive diseases also include anophthalmia, lethal sarcoidosis and red-green color blindness, which should be treated according to the doctor’s prescription.