Auricular Malformation: Causes, Symptoms & Treatment

An auricular malformation is characterized by abnormalities in the shape of the auricle. It often does not represent a disease value as in the case of protruding ears. However, severe auricular malformations may be an accompanying symptom of a syndrome with other physical malformations. What is an auricular malformation? The term auricular malformation includes both … Auricular Malformation: Causes, Symptoms & Treatment

Silver-Russell Syndrome: Causes, Symptoms & Treatment

Silver-Russell syndrome (RSR) represents a very rare syndrome that is characterized by prenatal growth disturbances with the development of short stature. So far, only about 400 cases of the disease have been documented. The presentation is highly variable, suggesting that it is not a uniform disorder. What is Silver-Russell syndrome? Silver-Russell syndrome is characterized by … Silver-Russell Syndrome: Causes, Symptoms & Treatment

Nasality Disorder: Causes, Symptoms & Treatment

Nasality disorders are hyper- or hyponasality and manifest themselves accordingly in open or closed nasal passages. In addition to organic causes such as inflammation, clefts, or tumors in the oropharynx, functional causes may be responsible for nasality disorder. Therapy consists of causative treatment and exercise therapy steps to direct the articulation airflow. What is a … Nasality Disorder: Causes, Symptoms & Treatment

Three-limb Thumb Polysyndactyly Syndrome: Causes, Symptoms & Treatment

Three-limbed thumb polysyndactyly syndrome is characterized by multimemberedness of the thumb, often associated with syndactyly and multimemberedness of the toes. The malformation syndrome arises on the basis of a genetic mutation and is inherited in an autosomal dominant manner, with expressivity subject to variability. Patients are treated by surgical amputation. What is three-limb thumb polysyndactyly … Three-limb Thumb Polysyndactyly Syndrome: Causes, Symptoms & Treatment

Dyschondrosteosis Léri Weill: Causes, Symptoms & Treatment

Dyschondrosteosis Léri Weill is a disorder with genetic causes. Dyschondrosteosis Léri Weill is classified in the category of skeletal dysplasias. The typical characteristic of the disease is short stature, which is also disproportionate. The middle sections of the extremities are symmetrically shortened. At the same time, a so-called Madelung deformity occurs in the context of … Dyschondrosteosis Léri Weill: Causes, Symptoms & Treatment