| Marshall syndrome | <syndrome> Syndrome of mid-face hypoplasia, cataract, sensorineural hearing loss, and hypohidrosis. It is disputed whether this syndrome is distinct from Stickler's syndrome. (05 Mar 2000) |
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| Marshall, Don | <person> U.S. Ophthalmologist, *1905. See: Marshall syndrome. (05 Mar 2000) |
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| Marshall, Eli | <person> U.S. Pharmacologist, 1889-1966. See: Marshall's method. (05 Mar 2000) |
| Marshall, John | <person> English anatomist, 1818-1891. See: Marshall's vestigial fold, Marshall's oblique vein. (05 Mar 2000) |
| Marshall-Marchetti-Krantz operation | An operation for urinary stress incontinence, performed retropubically. (05 Mar 2000) |
| Marshall-Marchetti test | Manual deviation of bladder neck during strain or cough to ascertain presence of stress urinary incontinence. Synonym: Bonney test, Marshall-Marchetti test. (05 Mar 2000) |
| Marshall's method | A quantitative procedure for estimating free and conjugated sulfanilamide in body fluids. (05 Mar 2000) |
| Marshall's oblique vein | A small vein on the posterior wall of the left atrium which merges with the great cardiac vein to form the coronary sinus; it is developed from the left common cardinal vein, and occasionally persists as a left superior vena cava. Synonym: vena obliqua atrii sinistri, Marshall's oblique vein. (05 Mar 2000) |
| Marshall's vestigial fold | A pericardial fold lying between the left oblique vein of the atrium and the left superior pulmonary vein containing the obliterated remains of the left superior vena cava. Synonym: plica venae cavae sinistrae, Marshall's vestigial fold, vestigial fold. (05 Mar 2000) |
| Marshall test | Manual deviation of bladder neck during strain or cough to ascertain presence of stress urinary incontinence. Synonym: Bonney test, Marshall-Marchetti test. (05 Mar 2000) |
| Marshall, Victor | <person> U.S. Urologist, *1913. See: Marshall-Marchetti-Krantz operation. (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) |
| Achard syndrome | <syndrome> Arachnodactyly with small receding mandible, broad skull, and joint laxity limited to the hands and feet; genetics unclear. (05 Mar 2000) |