| Fuchs' syndrome | <syndrome> A syndrome characterised by heterochromia of the iris, iridocyclitis, keratic precipitates, and cataract. Synonym: Fuchs' heterochromic cyclitis. (05 Mar 2000) |
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| angle of Fuchs | <ophthalmology> A crevice between the ciliary and pupillary zones of the iris formed by atrophy of superficial layers of the iris in the pupillary zone. (05 Mar 2000) |
| Dalen-Fuchs nodules | Collections of epithelial cells lying between Bruch's membrane and the retinal pigment epithelium in sympathetic ophthalmia and rarely in other granulomatous intraocular inflammations. (05 Mar 2000) |
| Fuchs' adenoma | <tumour> A benign epithelial tumour of the non-pigmented epithelium of the ciliary body, rarely exceeding 1 mm in diameter. (05 Mar 2000) |
| Fuchs' black spot | An area of pigment proliferation in the macular region in degenerative myopia. (05 Mar 2000) |
| Fuchs' coloboma | A congenital inferior crescent on the choroid at the edge of the optic disk; not associated with myopia. Synonym: congenital conus. (05 Mar 2000) |
| fuchs' endothelial dystrophy | Disorder caused by loss of endothelium of the central cornea. It is characterised by hyaline endothelial outgrowths on descemet's membrane, epithelial blisters, reduced vision, and pain. (12 Dec 1998) |
| Fuchs' epithelial dystrophy | Epithelial oedema secondary to endothelial dystrophy of the cornea. (05 Mar 2000) |
| Fuchs, Ernst | <person> Austrian ophthalmologist, 1851-1930. See: Fuchs' adenoma, angle of Fuchs, Fuchs' heterochromic cyclitis, Fuchs' coloboma, Fuchs' epithelial dystrophy, Fuchs' black spot, Fuchs' spur, Fuchs' stomas, Fuchs' syndrome, Fuchs' uveitis, Dalen-Fuchs nodules. (05 Mar 2000) |
| Fuchs' heterochromic cyclitis | <syndrome> A syndrome characterised by heterochromia of the iris, iridocyclitis, keratic precipitates, and cataract. Synonym: Fuchs' heterochromic cyclitis. (05 Mar 2000) |
| Fuchs' uveitis | Anterior uveitis and depigmentation of the iris. Synonym: Fuchs' uveitis. (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) |
| abstinence syndrome | <syndrome> A constellation of physiologic changes undergone by persons or animals who have become physically dependent on a drug or chemical due to prolonged use at elevated doses, but who are abruptly deprived of that substance. The abstinence syndrome varies with the drug to which dependence has developed. Generally the effects observed are in an opposite direction from those produced by the drug; e.g., the withdrawal syndrome from central nervous system depressants such as barbiturates and benzodiazepines consists of insomnia, restlessness, tremulousness, hallucinations, and, in the extreme, tonic-clonic convulsions which may prove fatal. The onset time and severity of the abstinence syndrome depend upon how rapidly the drug disappears from the body. (05 Mar 2000) |