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Dermatophagia (from Ancient Greek δέρμα — lit. skin and φαγεία lit. eating) or dermatodaxia (from δήξις, lit. biting) is a compulsion disorder of gnawing or biting one's own skin, most commonly at the fingers.
Biting the fingers and lips is a definitive feature of Lesch–Nyhan syndrome; in other syndromes associated with self-injury, the behaviors usually consist of head banging and nonspecific self-mutilation, but not biting of the cheeks, lips and fingers.
Signs and symptoms Compulsive picking of the knuckles (via mouth) illustrating potentially temporary disfiguration of the distal and proximal joints of the middle and little fingers. The fingers have been compulsively picked and chewed in someone with excoriation disorder and dermatophagia.
Russell's sign. Causes. The most common causes of Russell’s Sign are bulimia and anorexia nervosa. Diagnostic method. Russell's Sign can be used as a factor to diagnose bulimia nervosa or anorexia nervosa. Differential diagnosis. indirect sign of bulimia nervosa or anorexia nervosa. Deaths.
Symptoms. Common symptoms in humans include: Nail biting; Pulling hair; Chewing fingers (in extreme cases, leading to amputation) Possible causes. This section will focus on the causes for autophagia in humans. There is no single primary cause for autophagia.
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Nail biting, also known as onychophagy or onychophagia, is an oral compulsive habit of biting one's fingernails. It is sometimes described as a parafunctional activity, the common use of the mouth for an activity other than speaking, eating, or drinking.
Coffin–Lowry syndrome is an X-linked disorder resulting from loss-of-function mutations in the RPS6KA3 gene, which encodes RSK2 ( ribosomal S6 kinase 2). Multiple mutations have been identified in RPS6KA3 that can give rise to the disorder, including missense mutations, nonsense mutations, insertions and deletions.
Trichophagia is a form of disordered eating in which persons with the disorder suck on, chew, swallow, or otherwise eat hair. The term is derived from ancient Greek θρίξ, thrix ("hair") and φαγεῖν, phagein ("to eat").
Apert syndrome is a form of acrocephalosyndactyly, a congenital disorder characterized by malformations of the skull, face, hands and feet. It is classified as a branchial arch syndrome, affecting the first branchial (or pharyngeal) arch, the precursor of the maxilla and mandible. Disturbances in the development of the branchial arches in fetal ...
The skin between the fingers and toes may be fused (cutaneous syndactyly). This disorder is also characterized by widely spaced eyes (ocular hypertelorism), an abnormally large head size ( macrocephaly ), and a high, prominent forehead.