Search results
Results from the WOW.Com Content Network
Dermatophagia is a type of pica and a body-focused repetitive behavior that involves gnawing or biting one's own skin, usually at the fingers. It can be conscious or unconscious, and it may be related to other disorders such as OCD or autism.
Excoriation disorder, also known as dermatillomania or skin picking disorder, is a mental disorder that causes repeated picking at one's own skin. It can be triggered by stress, anxiety, or perceived skin defects, and can lead to physical damage, infection, and psychological distress.
Autophagia is the practice of biting or consuming one's own body, such as nails, hair or fingers. It is a sub category of self-injurious behavior and may be related to mental disorders, impulse control or pain seeking.
Psychomotor agitation is a symptom of various disorders and health conditions, such as schizophrenia, bipolar disorder, PTSD, and withdrawal. It involves unintentional and purposeless motions and restlessness, often accompanied by emotional distress. Pacing around is one of the typical manifestations of psychomotor agitation.
Learn about the types, causes, diagnosis, treatment and prevalence of BFRBs, impulse control disorders that involve damaging one's physical appearance or causing injury. BFRBs include skin picking, nail biting, hair pulling, nose picking and more.
Tardive tourettism is a tic disorder featuring the same symptoms as Tourette syndrome. The two disorders are extremely close in nature and often can only be differentiated by the details of their respective onsets. Tardive myoclonus, a rare disorder, presents as brief jerks of muscles in the face, neck, trunk, and extremities. [13]
Apert syndrome is a genetic disorder that causes malformations of the skull, face, hands and feet. It is a type of acrocephalosyndactyly, affecting the first branchial arch, and has three types of hand deformities: spade, mitten and rosebud.
Lesch–Nyhan syndrome (LNS) is a rare inherited disorder caused by a deficiency of the enzyme hypoxanthine-guanine phosphoribosyltransferase (HGPRT). This deficiency occurs due to mutations in the HPRT1 gene located on the X chromosome.