| HG | hand grip; herpes gestationis; Heschl's gyrus; high glucose; human gonadotropin; human growth; hypog... |
|---|---|
| HK | hand to knee; heat-killed; heel-to-knee; hexokinase; human kidney |
| H-K | hand to knee |
| HM | hand movements; health maintenance; heart murmur; hemifacial microsomia; Holter monitoring; home man... |
| HMC | hand-mirror cell; health maintenance cooperative; heroin, morphine, and cocaine; histocompatibility ... |
| obstetrical hand | Position of the hand in tetany or in muscular dystrophy; the fingers are flexed at the metacarpophalangeal joints and extended at the phalangeal joints, with the thumb flexed and adducted into the palm; in resemblance to the position of the physician's hand in making a vaginal examination. Synonym: main d'accoucheur, obstetrical hand. (05 Mar 2000) |
|---|---|
| one-hand | Employing one hand; as, the one-hand alphabet. See: dactylology. (04 Mar 1998) |
| opera-glass hand | A deformity of the hand seen in chronic absorptive arthritis, the fingers and wrists being shortened and the covering skin wrinkled into transverse folds; the phalanges appear to be retracted into one another like an opera glass or miniature telescope. Synonym: main en lorgnette. (05 Mar 2000) |
| EF hand | A very common calcium binding motif. A 12 amino acid loop with a 12 amino acid _ helix at either end, providing octahedral co-ordination for the calcium ion. Members of the family include: aequorin, _ actinin, calbindin, calcineurin, calcyphosin, calmodulin, calpain, calcyclin, iacylglycerol kinase, fimbrin, myosin regulatory light chains, oncomodulin, osteonectin, spectrin, troponin C. (18 Nov 1997) |
| trench hand | An obsolete term for frostbite of the hand. (05 Mar 2000) |
| trident hand | A hand in which the fingers are of nearly equal length and deflected at the first interphalangeal joint, so as to give a forklike shape; seen in achondroplasia. (05 Mar 2000) |
| two-hand | Employing two hangs; as, the two-hand alphabet. See Dactylology. Source: Websters Dictionary (01 Mar 1998) |
| joints of hand | These joints include the radiocarpal or wrist joint; intercarpal, carpometacarpal, intermetacarpal; metacarpophalangeal and interphalangeal joints. Synonym: articulationes manus, articulations of hand. (05 Mar 2000) |
| fibrous digital sheaths of hand | Fibrous sheaths of the digits of the hand, the tubular fibrous layers that enclose the synovial sheaths and the superficial and deep flexor tendons and the tendon of the flexor pollicis longus in their passage along their respective digits; they are composed of annular and cruciform parts. Synonym: vaginae fibrosae digitorum manus. (05 Mar 2000) |
| flat hand | Loss of normal arches of the hand. Synonym: flat hand. (05 Mar 2000) |
| flexor digiti minimi brevis muscle of hand | Origin, hamulus of hamate bone; insertion, medial side of proximal phalanx of little finger; action, flexes proximal phalanx of little finger; nerve supply, ulnar. Synonym: musculus flexor digiti minimi brevis manus, short flexor muscle of little finger. (05 Mar 2000) |
| free-hand knife | A manually operated knife or blade usually used to take split-thickness skin grafts; e.g., Blair-Brown knife, Humby knife, Theirsh knife. (05 Mar 2000) |
| lumbrical muscle of hand | Four intrinsic muscles of the hand; origin, the two lateral: from the radial side of the tendons of the flexor digitorum profundus going to the index and middle fingers; the two medial: from the adjacent sides of the second and third, and third and fourth tendons; insertion, radial side of extensor tendon on dorsum of each of the four fingers; action, flexes metacarpophalangeal joint and extends the proximal and distal interphalangeal joint; nerve supply, the two radial muscles by the median, the two ulnar muscles by the ulnar. Synonym: musculus lumbricalis manus. (05 Mar 2000) |
| adrenal hyperplasia, congenital | A group of inherited disorders of adrenal steroidogenesis, the physical expression of which varies with the sex of the patient, the severity of the congenital enzyme defect, and the age at which the defect makes its presence felt. The most common form, the simple virilizing form, is due to a 21-hydroxylase deficiency. There is also a salt-losing form (a more complete 21-hydroxylase deficiency), a hypertensive form (11-hydroxylase deficiency), a 17-hydroxylase deficiency form, a desmolase deficiency form, and a 3-beta-hydroxysteroid deficiency form. (12 Dec 1998) |
| anaemia, dyserythropoietic, congenital | A familial disorder characterised by anaemia with multinuclear erythroblasts, karyorrhexis, asynchrony of nuclear and cytoplasmic maturation, and various nuclear abnormalities of bone marrow erythrocyte precursors. Type II is the most common of the 3 types of congenital dyserythropoietic anaemia; it is often referred to as hempas, based on the hereditary erythroblast multinuclearity with positive acidified serum test. (12 Dec 1998) |