| 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) |
| Aarskog-Scott syndrome | A syndrome of ocular hypertelorism, anteverted nostrils, broad upper lip, saddle-bag scrotum, and laxity of ligaments resulting in genu recurvatum, flat feet, and hyperextensible fingers; X-linked and autosomal dominant forms. Synonym: Aarskog-Scott syndrome. (05 Mar 2000) |
| Aarskog syndrome | <syndrome> Grier et al. (1983) reported father and 2 sons with typical Aarskog syndrome, including short stature, hypertelorism, and shawl scrotum. They tabulated the findings in 82 previous cases. X-linked recessive inheritance has been repeatedly suggested. The family reported by Welch (1974) had affected males in 3 consecutive generations. Thus, there is either genetic heterogeneity or this is an autosomal dominant with strong sex-influence and possibly ascertainment bias resulting from use of the shawl scrotum as a main criterion. Stretchable skin was present in the cases of Grier et al. (1983). Teebi et al. (1993) reported the case of an affected mother and 4 sons (including a pair of monozygotic twins) by 2 different husbands. They suggested that the manifestations were as severe in the mother as in the sons and that this suggested autosomal dominant inheritance. Actually, the mother seemed less severely affected, compatible with X-linked inheritance. Clinical signs: Mild to moderate short stature,normocephaly, Widow's peak hair, maxillary hypoplasia, broad nasal bridge, anteverted nostrils, long philtrum, broad upper lip, curved linear dimple below the lower lip, hypertelorism, ptosis, down-slanted palpebral fissures, ophthalmoplegia, strabismus, hyperopic astigmatism, large cornea, floppy ears, lop-ears,cleft lip/palate, shawl scrotum, saddle-bag scrotum, cryptorchidism, brachydactyly, digital contractures, clinodactyly, mild syndactyly, transverse palmar crease, lymphoedema of the feet, ligamentous laxity, osteochondritis dissecans, proximal finger joint hyperextensibility, flexed distal finger joints, genu recurvatum, flat feet, stretchable skin, cervical spine hypermobility, odontoid anomaly, macrocytic anaemia, hemochromatosis, hepatomegaly, portal cirrhosis, imperforate anus, rectoperineal fistula, interstitial pulmonary disease, sternal deformity. Inheritance: Sex-influenced autosomal dominant form, also X-linked form. (05 Aug 1998) |
| abdominal muscle deficiency syndrome | <syndrome> Congenital absence (partial or complete) of abdominal muscles, in which the outline of the intestines is visible through the protruding abdominal wall; in males, genitourinary anomalies (urinary tract dilation and cryptorchidism) are also found; genetics unclear. (05 Mar 2000) |