| CPTH | chronic post-traumatic headache |
|---|---|
| CTH | ceramide trihexoside; chronic tension headache; cystathionase |
| HA | H antigen; Hakim-Adams [syndrome]; halothane anesthesia; Hartley [guinea pig]; headache; health alli... |
| H/A | head to abdomen; headache |
| HID | headache, insomnia, depression [syndrome]; herniated intervertebral disc; human infectious dose; hyp... |
| periodic catatonia | Regularly reappearing phases of catatonic excitement. (05 Mar 2000) |
|---|---|
| periodic disease | A condition characterised by regularly recurring and intermittent episodes of fever, oedema, arthralgia, and gastric pain and vomiting, continuing for years without further development in otherwise healthy individuals. It is also called familial mediterranean fever. It does not refer to conditions in which episodes recur at regular intervals. (12 Dec 1998) |
| periodic fever | An obsolete term introduced to describe the intermittent febrile episodes seen in disease later recognised and named familial Mediterranean fever. (05 Mar 2000) |
| periodic filariasis | A form of filariasis in which microfilariae appear in the peripheral blood at regular 24-hr intervals; usually refers to the nocturnal periodicity of bancroftian filariasis. (05 Mar 2000) |
| periodic law | The properties of elements are periodical functions of their atomic weights; i.e., if the elements are arranged in the order of their atomic weights, every element in the series will be related in respect to its properties to the eighth in order before or after it. Synonym: periodic law. (05 Mar 2000) |
| periodic migrainous neuralgia | Recurrent facial pain and headache, more common in men than in women. Synonym: Harris' migraine. (05 Mar 2000) |
| periodic neutropenia | Neutropenia recurring at regular intervals (14 to 45 days), in association with various types of infectious diseases, e.g., stomatitis, cutaneous ulcers, furuncles, arthritis, and others. Synonym: cyclic neutropenia. (05 Mar 2000) |
| periodic oedema | A vascular reaction involving the deep dermis or subcutaneous or submucal tissues, representing localised oedema caused by dilatation and increased permeability of the capillaries and characterised by development of giant wheals. (18 Nov 1997) |
| periodic ophthalmia | An acute iridocyclitis of horses, involving one or both eyes; it subsides only to recur at intervals of varying length and usually ends in blindness; the cause is uncertain but some have associated it with leptospires; does not appear to be contagious. Synonym: moon blindness. (05 Mar 2000) |
| periodic paralysis | Term for a group of diseases characterised by recurring episodes of muscular weakness or flaccid paralysis without loss of consciousness, speech, or sensation; attacks begin when the patient is at rest, and there is apparent good health between attacks. See: hyperkalaemic periodic paralysis, hypokalaemic periodic paralysis, normokalaemic periodic paralysis. (05 Mar 2000) |
| periodic peritonitis | familial paroxysmal polyserositis |
| periodic polyserositis | familial paroxysmal polyserositis |
| periodic system | The arrangement of the chemical elements in a definite order as indicated by their respective atomic numbers in such a way that groups of elements with similar chemical properties (similar valence shell electron number) are grouped together. See: Mendeleeff's law. (05 Mar 2000) |
| hyperkalaemic periodic paralysis | A form of periodic paralysis in which the serum potassium level is elevated during attacks; onset occurs in infancy, attacks are frequent but relatively mild, and myotonia is often present; autosomal dominant inheritance. (05 Mar 2000) |
| hypokalaemic periodic paralysis | <biochemistry> A rare inherited disorder, affecting men more often than women, characterised by intermittent episodes of muscle weakness or paralysis. One form, known as hypokalaemic periodic paralysis, is an autosomal recessive disorder that is characterised by bouts of muscle weakness (or paralysis) accompanied by low serum potassium levels. Inheritance: autosomal recessive. Incidence: 1 in 100,000. (11 Jan 1998) |