Urbach-Wiethe disease is a rare genetic disorder that can cause calcification of brain tissue in the temporal lobes; this calcification can cause damage to the amygdalae.
<h3>What are the symptoms of Urbach-Wiethe disease?</h3>
The symptoms of the disease vary greatly from individual to individual.
They may include a hoarse voice, lesions and scarring on the skin, easily damaged skin with poor wound healing, dry, wrinkly skin, and beading of the papules around the eyelids.
<h3>What part of the brain does Urbach-Wiethe disease affect?</h3>
(1994, 1995) investigated a patient suffering from Urbach–Wiethe (UW) syndrome, a very rare autosomal recessive disease, which produces bilateral calcifications in the anterior medial temporal lobes, especially of the amygdalae, in 50–75% of cases (Newton et al., 1971; Staut and Naidich, 1998).
Learn more about Urbach-Wiethe disease here:
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brainly.com/question/7224949</h3><h3 /><h3>#SPJ4</h3>
Because they all have something to do with animals ad what they eat.
The Golgi apparatus deals with packing of the cell!
Answer:
Hypothalamic-pituitary-adrenal axis (HPA axis)
Explanation:
- The three-stage process describing the physiological changes that take place in the body when it is under stress is known as general adaptation syndrome (GAS).
- The model describing the three-stage process was given by the scientist Hans Selye.
- According to this model, the responses in the body that occur during stress is regulated by the Hypothalamic-pituitary-adrenal axis (HPA axis) where the brain senses the stress and then the signals travel from the hypothalamus to the pituitary and finally the body releases cortisol from adrenal glands that contributes to the various changes.
