Frederick Walker Mott

Frederick Walker Mott

Summary

Portrait of Frederick Walker Mott Frederick Walker Mott 1911 Encyclopædia Britannica (1911)

In some cases there is a continual nodding movement of the head. These tremors are at the rate of five per second and cease during sleep. The attitude and gait are very characteristic; the head is bent forward, and the patient in beginning to walk takes slow steps, which soon become short and quick as if he were running after his centre of gravity. The intellect is clear and in marked contrast to the mask-like expression. This disease lasts for years, and but little can be done in the way of treatment, except passive movements of the limb to prevent contracture.
Source: Wikisource

Portrait of Frederick Walker Mott Frederick Walker Mott 1911 Encyclopædia Britannica (1911)

Paralyses—termed medically muscular dystrophies—may arise from a primary atrophy of muscle apparently independent of any discoverable change in the nervous system, but due to a congenital developmental defect of the muscles. Heredity plays an important part in the incidence of these diseases, members of the same family being affected with the same type of disease, and at the same period of life. There may be a tendency in a family to the affection of one sex and not the other
Source: Wikisource

Portrait of Frederick Walker Mott Frederick Walker Mott 1911 Encyclopædia Britannica (1911)

It is curious that the majority of cases are males, and that it is transmitted by women who are not themselves its subjects. Many different clinical types have been described based upon the age of onset, the groups of muscles first affected, and the presence or absence of apparent hypertrophy; they are however all varieties of one affection, and in a case where there is an apparent enlargement of muscles there is really atrophy of the contractile muscle, fibres and overgrowth of fat and interstitial fibrous tissue; consequently this form of the disease is called pseudo-kypertrophic paralysis.
Source: Wikisource

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