Lymphatic diathesis is not a disease, but a constitutional predisposition that favors the development of certain diseases. This predisposition is also known as lymphatism or exudative lymphatic diathesis. What is lymphatic diathesis? Lymphatic diathesis is a concept more common in naturopathic medicine than in conventional medicine. Lymphatic diathesis is not a disease in its own … Lymphatic Diathesis: Causes, Symptoms & Treatment
Chronic infantile neuro-cutaneo-articular syndrome (CINCA syndrome) is an autoinflammatory disorder that causes a spurious inflammatory response in the body. The syndrome manifests itself in infancy, including fever, pain, and neurological symptoms. Treatment is with the help of drugs that reduce the protein interleukin-1β. What is CINCA syndrome? The term chronic infantile neuro-cutaneo-articular syndrome (CINCA syndrome) … CINCA Syndrome: Causes, Symptoms & Treatment
Brown-Vialetto-Van Laere syndrome is a disease that is inherited. As part of the disease, the function of various caudal nerves in the brain is lost. Furthermore, affected patients lose their sense of hearing. In addition, a so-called spinal atrophy of the musculature develops in some of the affected individuals. What is Brown-Vialetto-Van Laere syndrome? Brown-Vialetto-Van … Brown-Vialetto-Van Laere Syndrome: Causes, Symptoms & Treatment
MUTYH-associated polyposis is closely related to adenomatous familial polyposis and is caused by a genetic mutation. Patients suffer from multiple colon polyps with risk of degeneration. Regular colonoscopies are mandatory. What is MUTYH-associated polyposis? Polyposis is polyp disease in hollow organs. Polyps are outpouchings of the mucosa that occur more frequently in the gastrointestinal tract, … MUTYH-associated Polyposis: Causes, Symptoms & Treatment
Juvenile stage refers to the stage of a living being after birth and before sexual maturity. After that, they are considered adults (adolescence); before that, they are in the embryonic stage. In humans, the juvenile phase goes from infancy to early adolescence (pubescence). What is the juvenile stage? The juvenile phase refers to the phase … Juvenile Phase: Function, Tasks, Role & Diseases
Tuberous sclerosis is a hereditary disease associated with various malformations of the brain and skin changes. The condition is also known as Bourneville-Pringle syndrome after its discoverers. What is tuberous sclerosis? Tuberous sclerosis is called tuberous sclerosis complex (TSC) in English. The disease belongs to the group of phakomatoses. Phakomatoses are diseases characterized by malformations … Tuberous Sclerosis: Causes, Symptoms & Treatment
Günther’s disease is an autosomal recessive inherited gene mutation of chromosome ten. The disease disrupts enzyme activity and the biosynthesis of heme into red blood pigment. Anemia and photosensitivity are among the major symptoms. What is Guenther’s disease? Günther’s disease is understood by physicians to be a rare inherited disorder. The disease is also known … Guenthers Disease: Causes, Symptoms & Treatment
Clouston syndrome is a type of ectodermal dysplasia. It is caused by an autosomal dominant inherited mutation. No causative treatment is available. What is Clouston syndrome? Dysplasias are malformations in various tissues. The heterogeneous disease group of ectodermal dysplasia includes inherited defects associated with malformations of structures from the outer cotyledon. The outer cotyledon of … Clouston Syndrome: Causes, Symptoms & Treatment
The lips, one of the most important sensory organs in humans, are used for articulation, food intake, facial expression. A tumor in this area is associated with significant impairment in functioning. In most cases, it is a malignant form of a tumor. However, if lip cancer is diagnosed at an early stage, there is a … Lip Cancer: Causes, Symptoms & Treatment
Mandibuloacral dysplasia is a congenital malformation syndrome associated with abnormalities of the skeleton that is inherited in an autosomal recessive manner. Two different types of the disease are known, caused by mutations in two different genes. A causative therapy does not yet exist. What is mandibuloacral dysplasia? In medicine, dysplasias are congenital malformations in human … Mandibuloacral Dysplasia: Causes, Symptoms & Treatment
TAR syndrome, Thrombocytopenia-Absent Radius Syndrome in English, is understood by medical science to be a malformation syndrome whose leading symptoms include nonunion of the spokes and thrombocytopenia. The cause of the syndrome is probably a hereditary gene mutation. Treatment consists primarily of platelet transfusion during the first few years of life. What is TAR syndrome? … TAR Syndrome: Causes, Symptoms & Treatment
Madelung deformity is a growth disorder of the forearm that results in a malpositioned arm and an abnormally long ulna. The patient’s bone formation is disturbed, causing dysostosis, which usually becomes noticeable in adolescence as a result of weight-bearing. The deformity can be corrected surgically. What is a Madelung deformity? Madelung deformity belongs to the … Madelung Deformity: Causes, Symptoms & Treatment
