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1.
Arch Toxicol ; 77(10): 601-4, 2003 Oct.
Article in English | MEDLINE | ID: mdl-14574449

ABSTRACT

A report of seven people who accidentally drank a juice contaminated with CS (o-chlorobenzylidene malononitrile) is given. Due to its mucosal irritating properties, CS (also known as "tear gas") is commonly used by policemen and soldiers in riot control. However, only a few reports of its ingestion by humans exist. Ingestion of CS may cause immediate irritation of the oral mucosa and gastrointestinal symptoms later on. Damage of internal organs, which has been shown in animals but only rarely in humans, is probably related to the dose ingested. The extensive use of CS gas merits recognition of the signs and symptoms of its exposure in order to reduce anxiety in both patients and medical staff and to facilitate fast and efficient management.


Subject(s)
Riot Control Agents, Chemical/poisoning , o-Chlorobenzylidenemalonitrile/poisoning , Adult , Beverages/poisoning , Female , Humans , Male , Riot Control Agents, Chemical/metabolism , o-Chlorobenzylidenemalonitrile/metabolism
2.
Am J Med Genet ; 80(2): 173-6, 1998 Nov 02.
Article in English | MEDLINE | ID: mdl-9805137

ABSTRACT

Cystinuria is a hereditary disorder manifested by the development of kidney stones. Three subtypes of the disease have been described, based on urinary excretion of cystine and the dibasic amino acids in heterozygotes, and oral loading tests in homozygotes. Cystinuria is very common among Libyan Jews living in Israel. Recently, we mapped the disease-causing gene in Libyan Jews to 19q, and have shown a very strong founder effect. In this report we present the results of biochemical and clinical studies performed on Libyan Jewish cystinuria patients and members of their families. High levels of cystine and the dibasic amino acids in heterozygotes support previous data that cystinuria in Libyan Jews is a non-type I disease. Oral loading tests performed with lysine showed some degree of intestinal absorption, but less than in normal controls. Previous criteria for determining the disease type, based solely on urinary amino acid levels, proved useless due to a very wide range of cystine and the dibasic amino acids excreted by the heterozygotes. Urinary cystine levels were useful in distinguishing between unaffected relatives and heterozygotes, but were unhelpful in differentiating between heterozygotes and homozygotes. Urinary levels of ornithine or arginine, and the sum of urinary cystine and the dibasic amino acids, could distinguish between the last two groups. Among stone formers, 90% were homozygotes and 10% were heterozygotes; 15% of the homozygotes were asymptomatic.


Subject(s)
Cystinuria/metabolism , Jews , Chromosome Mapping , Chromosomes, Human, Pair 19 , Cystinuria/ethnology , Cystinuria/genetics , Cystinuria/pathology , Heterozygote , Homozygote , Humans , Libya/ethnology
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