Trisomy 13, also known as Pätau syndrome, is a rare genetic defect in which chromosome 13 occurs three times instead of the usual two. It leads to a variety of different diseases and physical characteristics, most of which result in death in early childhood. Trisomy 13 is one of the best known triple abnormalities after … Trisomy 13 (Paetau Syndrome): Causes, Symptoms & Treatment
Trisomy 14 is the result of a genomic mutation. Symptoms depend on the type of mutation. Often, trisomy 14 causes miscarriages, according to studies. What is trisomy 14? There is a difference between gene mutations and genomic mutations. In gene mutations, certain nucleotides are missing, some nucleotides are switched, or additional nucleotides are added. In … Trisomy 14: Causes, Symptoms & Treatment
Treacher-Collins syndrome is the name given to an inherited disorder that causes facial deformities. The condition is now often referred to as Franceschetti-Zwahlen syndrome, Berry syndrome, or dysostosis mandibulofacialis. The formations of the malformations caused by the syndrome are highly variable, but often involve the chin, eyes, ears, palate, or zygomatic bone. What is Treacher-Collins … Treacher Collins Syndrome: Causes, Symptoms & Treatment
The levator veli palatini muscle has an important function in the swallowing process. It is part of the muscles of the pharynx. It prevents food or liquids from flowing into the nasal cavity. What is the levator veli palatini muscle? The levator veli palatini muscle is located in the human head. It is a part … Musculus Levator Veli Palatini: Structure, Function & Diseases
The term articulation disorder refers to various problems in a person’s individual sound formation that deviate from the standard. This means that certain sounds are either not formed at all or are formed incorrectly. The causes of an articulation disorder can be very diverse, and treatment is usually provided by a speech therapist. What are … Articulation Disorder: Causes, Symptoms & Treatment
Pena-Shokeir syndrome is a serious genetic disorder with multiple malformations of internal and external organs. If the infants are born alive, death occurs after a few days or weeks at the latest. The main cause of death is severe pulmonary hypoplasia. What is Pena-Shokeir syndrome? Pena-Shokeir syndrome is a very rare serious disorder characterized by … Pena-Shokeir Syndrome: Causes, Symptoms & Treatment
Ellis-van Creveld syndrome is an extremely rare genetic disorder. It is characterized by short ribs and polydactyly (multiple fingers). Life expectancy depends on the size of the thorax and the severity of any heart defect. What is Ellis van Creveld syndrome? Ellis-van Creveld syndrome is also known as chondroectodermal dysplasia because of the involvement of … Ellis Van Creveld Syndrome: Causes, Symptoms & Treatment
