Sensenbrenner syndrome is a genetic disorder that is extremely rare. Sensenbrenner syndrome is characterized by a variety of anatomical and functional defects. Currently, there are fewer than 20 known cases of Sensenbrenner syndrome. A first description of Sensenbrenner syndrome was given in 1975. What is Sensenbrenner syndrome? Sensenbrenner syndrome is an inherited disorder, with an … Sensenbrenner Syndrome: Causes, Symptoms & Treatment
Johanson-Blizzard syndrome is the name given to a hereditary disease that is rare. Affected individuals suffer from developmental abnormalities of the pancreas, scalp and nose. What is Johanson-Blizzard syndrome? Johanson-Blizzard Syndrome (JBS) is a rare inherited disorder that can sometimes be fatal. The syndrome is also considered ectodermal dysplasia and is classified as a pancreatic … Johanson Blizzard Syndrome: Causes, Symptoms & Treatment
EEC syndrome is a rare condition that is present at birth. The abbreviation stands for the terms ectrodactyly, ectodermal dysplasia and cleft (English name for cleft lip and palate). Thus, the disease term summarizes the three most important symptoms of EEC syndrome. Patients suffer from a cleft hand or foot and defects of ectodermal dysplasia. … EEC Syndrome: Causes, Symptoms & Treatment
Limb mammary syndrome is a condition that belongs to the category of ectodermal dysplasias. Limb mammary syndrome is already present at birth in affected individuals. The disease is known by the abbreviation LMS and occurs comparatively rarely. Limb mammary syndrome is typically characterized by marked anatomic malformations of the feet and hands in association with … Limb Mammary Syndrome: Causes, Symptoms & Treatment
Hay-Wells syndrome is a hereditary disease caused by a gene mutation of the TP63 gene. In addition to changes in the appearance of the skin, this disease primarily causes maldevelopment of the skin appendages and teeth. Treatment of the disease itself is not possible, but therapy of the corresponding symptoms is. What is Hay-Wells syndrome? … Hay-Wells Syndrome: Causes, Symptoms & Treatment
Ectodermal dysplasia is a group of genetic malformations of tissues and body parts that arise from the ectoderm. The common abbreviation of ectodermal dysplasia is ED. The term stands for a variety of diseases and pathological disorders, especially of the nails, hair, skin, sweat glands and teeth. Ectodermal dysplasia occurs, for example, in Ellis-van Creveld … Ectodermal Dysplasia: Causes, Symptoms & Treatment
