Kennedy disease is a male affliction that also disrupts the transfer of neurons between the brain and spinal motor neurons, causing progressive paralysis, and the usual symptoms begin between 20 and 40 years.
According to the medical website, the first symptoms include shaking hands, twitching of the muscles, muscle cramps followed by weakness in the shoulder or hip, limb breasts, weak facial or facial tongue, speech, difficulty in swallowing, causing frequent episodes of pneumonia, complications include diabetes, gynaecomastia and infertility.
Way of inheritance
The mother of the patient has one copy of a transgenic gene that is transferred to the son, the mother is a carrier but not affected and has a 50% chance of passing the abnormal gene of one of her descendants. Also, but do not show symptoms, they become vectors like them.
Diagnosis and treatment
Diagnosis is done through clinical signs and genetic tests, and treatment can only involve physiotherapy and rehabilitation methods to improve the strength of current muscles, which aims to slow down worsening and paralysis.
Paralysis usually permeates so that people with the disease can move later when they are forced to use wheelchairs, and monitoring of pulmonary function and muscle strength is required to assess the progression of the disease.