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1. are those that have a low prevalence in the population. To be considered rare, each specific disease can only affect a limited number of people

2. Amyotrophic Lateral Sclerosis

   • it destroys the motor neurons that are an important link in the nervous system,
     • • Go from being a healthy and strong person, with developed muscles, to lose your muscle mass and remain in a compulsory wheelchair
   • which through the brain control the voluntary movements of the body and provide the information for the nutrition of the muscles

3. Acrogeria Gottron

   • It mainly affects women, characterized by skin atrophy and loss of subcutaneous fat from the beginning to the birth or soon after.
   • The extremities, backs of the hands and feet are particularly affected, but changes may also appear on the face and trunk.
     • The skin is thin, dry and transparent. The nails are dystrophic, fine hair without baldness, it has no systemic repercussions and the physical and mental development is normal.

4. Autosomal recessive mutation dRTA

   • It is an inherited form of distal renal tubular acidosis (RTA) characterized by hyperkalemic hypokalemic metabolic acidosis.
     • This gene is a unit that controls listening at an early age and in some cases at a late age, if it is affected it leaves the affected person with little or no audio.
       • • It is not demonstrated in any way, it only appears and harm your life

5. Angioneurotic edema

   • It is characterized by rapid swelling (edema) of the skin, mucosa, and submucosal tissues. Aside from its common allergy-induced form, it has been reported as a side effect of some medications, especially ACE inhibitors.
     • Mucus practically all the time, allergy and watery eyes and on many occasions swollen. The allergy will probably cause pain to those who suffer it, in addition to the fact that the eyes become blurred with the eyes made.
       • • Allergy is the most painful, but to cloud my eyesight is the most uncomfortable, not seeing in the morning is horrible

6. Hypomyelinating leukodystrophy

   • A rare hypomyelinating leukodystrophy disorder characterized by the association of dental abnormalities,
   • hypogonadotropic hypogonadism, and hypomyelinating leukodystrophy manifesting with delayed or regression of neurological development and / or progressive cerebellar symptoms.
     • Signs frequently include intentional tremor, dysmetry, lack of smooth follow-up and gaze-evoked nystagmus, and, more variably, gait ataxia and vertical gaze limitation.

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