Search results
Results From The WOW.Com Content Network
Triangular Interval Syndrome (TIS) was described as a differential diagnosis for radicular pain in the upper extremity. [6] It is a condition where the radial nerve is entrapped in the triangular interval resulting in upper extremity radicular pain. The radial nerve and profunda brachii pass through the triangular interval and are hence vulnerable.
The triangular space (also known as the medial triangular space, [1] upper triangular space, [2] medial axillary space or foramen omotricipitale [3]) is one of the three spaces found at the axillary space. The other two spaces are the quadrangular space and the triangular interval. [4]
SOFT syndrome, also known for the name its acronym originates from: Short stature-onychodysplasia-facial dysmorphism-hypotrichosis syndrome, is a rare genetic disorder characterized by the presence of short stature, underdeveloped nails, facial dysmorphisms (such as long triangular face, down-slanting palpebral fissures, etc.), and hair sparcity across the body. [1]
Quadrilateral space syndrome is a rotator cuff denervation syndrome in which the axillary nerve is compressed at the quadrilateral space of the rotator cuff. Cause [ edit ]
Ænglisc; Аԥсшәа; العربية; Azərbaycanca; تۆرکجه; বাংলা; Banjar; Беларуская (тарашкевіца) Bosanski; Català; Čeština
Printable version; In other projects Appearance. move to sidebar hide. From Wikipedia, the free encyclopedia. Redirect page. Redirect to: Triangular interval;
Joubert syndrome often manifests with similar cerebellar hypoplasia and its sequelae, including hyperpnea, ataxia, changes in eye movement, and cleft lip and palate. Occasionally, Joubert syndrome will include heart malformations. Brachmann–de Lange syndrome must also be differentiated from 3C syndrome. It presents with similar craniofacial ...
TRIANGLE disease is a rare genetic disorder of the immune system. TRIANGLE stands for "TPPII-related immunodeficiency , autoimmunity , and neurodevelopmental delay with impaired glycolysis and lysosomal expansion" where TPP2 is the causative gene.