Vitiligo is an autoimmune acquired hypomelanosis, which has an important genetic component and is usually associated with other environmental triggers. It`s typical clinic manifestation of hypochromic or achromic macules with progressive behavior make it a relatively easy diagnosis. Vitiligo usually affects visible areas of the body having an important emotional impact for the patients, so psychological therapy is essential for the management of the disease. The treatment is oriented to stop the progression of the disease, help repigmentation and avoid relapses through the use of topical steroids, systemic steroids and phototherapy, with the final goal of improving quality of life.El vitíligo es una&n...
Systemic lupus is an autoimmune disease of unknown etiology, which causes an alteration of the immun...
Rheumatic fever is the result of the body's autoimmune response to a pharyngeal infection caused by ...
The PTEN gene, better known as PTEN tyrosine phosphatase, is a tumor suppressor gene on chromosome 1...
Vogt-Koyanagi-Harada Syndrome refers to an idiopathic, multisystemic and autoimmune disease, which c...
Developmental hip dysplasia is the most common orthopedic disorder in newborns; refers to a wide spe...
Hidradenitis suppurativa or reverse acne is a chronic inflammatory disease of the skin that affects ...
Vitiligo is considered a genetic susceptibility disorder, characterized by skin depigmentation due t...
Syncope is a loss of the state of consciousness that is characterized by being transient and self-li...
The opsoclonus-myoclonus syndrome is a rare medical condition associated with an autounmmune etiolog...
Inflammatory myopathies have an increased risk of malignancy, the one with the highest association b...
Eosinophilic esophagitis is a chronic disease mediated by the immune system, which is largely based ...
Eosinophilic esophagitis is characterized by the infiltration of eosinophils into the esophagus and ...
Periorbital edema is a clinical sign that presents a variety of causes, which should be considered d...
Primary dysmenorrhea is the most common symptom associated with menstruation and can be classified i...
Avascular necrosis of the femoral head is a multifactorial pathology characterized by the progressiv...
Systemic lupus is an autoimmune disease of unknown etiology, which causes an alteration of the immun...
Rheumatic fever is the result of the body's autoimmune response to a pharyngeal infection caused by ...
The PTEN gene, better known as PTEN tyrosine phosphatase, is a tumor suppressor gene on chromosome 1...
Vogt-Koyanagi-Harada Syndrome refers to an idiopathic, multisystemic and autoimmune disease, which c...
Developmental hip dysplasia is the most common orthopedic disorder in newborns; refers to a wide spe...
Hidradenitis suppurativa or reverse acne is a chronic inflammatory disease of the skin that affects ...
Vitiligo is considered a genetic susceptibility disorder, characterized by skin depigmentation due t...
Syncope is a loss of the state of consciousness that is characterized by being transient and self-li...
The opsoclonus-myoclonus syndrome is a rare medical condition associated with an autounmmune etiolog...
Inflammatory myopathies have an increased risk of malignancy, the one with the highest association b...
Eosinophilic esophagitis is a chronic disease mediated by the immune system, which is largely based ...
Eosinophilic esophagitis is characterized by the infiltration of eosinophils into the esophagus and ...
Periorbital edema is a clinical sign that presents a variety of causes, which should be considered d...
Primary dysmenorrhea is the most common symptom associated with menstruation and can be classified i...
Avascular necrosis of the femoral head is a multifactorial pathology characterized by the progressiv...
Systemic lupus is an autoimmune disease of unknown etiology, which causes an alteration of the immun...
Rheumatic fever is the result of the body's autoimmune response to a pharyngeal infection caused by ...
The PTEN gene, better known as PTEN tyrosine phosphatase, is a tumor suppressor gene on chromosome 1...