| duane's syndrome | <syndrome> A hereditary congenital syndrome in which the affected eye shows limitation or absence of abduction, restriction of adduction, retraction of the globe on adduction, narrowing of the palpebral fissure on adduction and widening on adduction, and deficient convergence. It is transmitted as an autosomal trait. (12 Dec 1998) |
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| Duane | Alexander, U.S. Ophthalmologist, 1858-1926. See: Duane's syndrome. (05 Mar 2000) |
| vertical retraction syndrome | <syndrome> A retraction of the globe and pseudoptosis on attempted adduction; due to co-innervation of the horizontal recti. Sometimes there is an inability to abduct the affected eye (type 1), or adduct the affected eye (type 2), or both (type 3). Synonym: Duane's syndrome. (05 Mar 2000) |
| retraction syndrome | <syndrome> A retraction of the globe and pseudoptosis on attempted adduction; due to co-innervation of the horizontal recti. Sometimes there is an inability to abduct the affected eye (type 1), or adduct the affected eye (type 2), or both (type 3). Synonym: Duane's syndrome. (05 Mar 2000) |
| gingival retraction | Lateral movement of the gingival margin away from the tooth surface; may be indicative of underlying inflammation or pocket formation, displacement of the marginal gingivae away from the tooth by mechanical, chemical, or surgical means. Mandibular retraction, a type of facial anomaly in which the gnathion lies posterior to the orbital plane. (05 Mar 2000) |
| pathologic retraction ring | A constriction located at the junction of the thinned lower uterine segment with the thick retracted upper uterine segment, resulting from obstructed labour; this is one of the classic signs of threatened rupture of the uterus. Synonym: Bandl's ring, Baudelocque's uterine circle, Scanzoni's second os. (05 Mar 2000) |
| retraction | 1. The act of drawing back, the condition of being drawn back. 2. Distal movement of teeth, usually accomplished with an orthodontic appliance. Origin: L. Retrahere = to draw back (18 Nov 1997) |
| retraction fibre | Thin projections from crawling cells associated with areas where the cell body is becoming detached from the substratum, but focal adhesions persist. Usually contain a bundle of microfilaments that are under tension. (18 Nov 1997) |
| retraction of publication | A statement issued by one or more authors of an article or a book, withdrawing or disavowing acknowledgment of their participation in performing research or writing the results of their study. In indexing, the retraction is sent to the editor of the publication in which the article appeared and is published under the rubric "retraction" or in the form of a letter. This publication type designates the author's statement of retraction: it should be differentiated from retracted publication which labels the retracted publication. (12 Dec 1998) |
| clot retraction | Retraction of a clot resulting from contraction of platelet pseudopods attached to fibrin strands that is dependent on the contractile protein thrombosthenin. Used as a measure of platelet function. (12 Dec 1998) |
| clot retraction time | The time required for a blood clot to separate from the tube wall and express serum, usually completed in 18 to 24 hours, but retarded or absent in persons with thrombocytopenic purpura. (05 Mar 2000) |
| physiologic retraction ring | A ridge on the inner uterine surface at the boundary line between the upper and lower uterine segment that occurs in the course of normal labour. (05 Mar 2000) |
| convergence-retraction nystagmus | Irregular, jerky nystagmus combining convergence and retraction of the eye into the orbit, especially on attempting an upward gaze. Synonym: Koerber-Salus-Elschnig syndrome. (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) |