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Biomedical subjects

J Israel

Publications and source records attributed to J Israel.

At least 37 records · Page 2Linked to original sources

Genetic counseling of the deaf. Medical and cultural considerations.

Genetic counseling is a communication process where information is provided in a nondirective way. Genetic counseling emphasizes informed decision making and provision of medical, psychological, and social support; genetic counseling is not advice giving. Individuals who are members of the deaf community (culturally deaf) present unique challenges to the ability of genetic counselors to be nondirective. In contrast to the medical model which considers deafness to be a pathological condition, many deaf people do not consider themselves to be handicapped but define themselves as being part of a distinct cultural group with its own language, customs, and beliefs. Cultural and linguistic factors have a strong influence on the success of genetic counseling with deaf people. Strategies for effective genetic counseling to deaf people include the recognition that perception of "risk" is very subjective and that some deaf individuals may prefer to have deaf children. Other considerations for successful service provision include the use of appropriate questionnaires or history-taking tools, the use of qualified interpreters, and the revision of counseling materials and terminology to eliminate cultural bias. Nondirective counseling is also very dependent on the educational background and level of understanding of the consultants. There is a desperate need for education within the deaf community about genetics, particularly the less well educated, and a need for training of genetic counselors who have an appreciation of the linguistic and cultural differences of the deaf. Additionally, as with any other cultural, racial, or ethnic group, it would be very appropriate for deaf persons to be trained as genetic counselors to provide genetic counseling to deaf people. Unfortunately, there are at present no culturally deaf genetic counselors in the United States. Genetic counseling for deaf couples can also be complicated by complex family trees with mating between several deaf people and by the potential presence of other complicating features that may be associated with syndromic types of deafness. This requires careful history taking by trained geneticists and often long, complex explanations to families when the mode of inheritance cannot be confirmed. Even though deaf people most often do not pursue genetic counseling because of concerns for reproductive outcome, there is great enthusiasm among members of the deaf community about genetic services when they are provided in a manner that is sensitive to their linguistic and cultural differences. Genetic counseling for culturally deaf people can have great personal benefits for these individuals, can increase general knowledge regarding hereditary types of deafness and can help in developing strategies for providing appropriate genetic counseling for individuals with all degrees of hearing loss.

Adult↗

Epidemic dropsy in Andhra Pradesh due to contaminated ghee.

An outbreak of epidemic dropsy in Andhra Pradesh was studied during August to September 1987. Thirty cases from 6 families were identified and examined. Ghee and one oil sample were found to be contaminated with the toxic compound sanguinarine. The affected families had purchased ghee from one vendor. The epidemic ended after alerting the villagers of the contaminated ghee, and stopping its further use.

Alkaloids↗

Disappearance of a sessile tubulovillous adenoma in the rectosigmoid colon during radiation therapy for cervical carcinoma.

Colonoscopic polypectomy is the usual treatment for an adenomatous colorectal polyp. We report a case of a sessile tubulovillous adenoma in the rectosigmoid colon disappearing during a course of radiation therapy for an unrelated cervical cancer. This case report illustrates that at least some colonic polyps are radiosensitive and can be eradicated during radiation therapy.

Adenoma↗

Interstitial and terminal deletions of the long arm of chromosome 4: further delineation of phenotypes.

We reviewed 45 patients with a deletion of the long arm of chromosome 4. Forty-one were previous reports (25 terminal deletions and 16 interstitial deletions) and 4 are new cases with terminal deletions. Of the 29 patients with terminal deletions, 18 with deletion at 4q31 and 4 at 4q32----qter had an identifiable phenotype consisting of abnormal skull shape, hypertelorism, cleft palate, apparently low-set abnormal pinnae, short nose with abnormal bridge, virtually pathognomonic pointed fifth finger and nail, congenital heart and genitourinary defects, moderate-severe mental retardation, poor postnatal growth, and hypotonia. Six patients with a deletion at 4q33 and one patient with deletion 4q34 were less severely affected. In general, patients with various interstitial deletions proximal to 4q31 had a phenotype that was less specific, although mental retardation and minor craniofacial anomalies were also present. There were 3 patients with piebaldism and one with Rieger syndrome. We conclude that terminal deletion of chromosome 4q (4q31----qter) appears to produce a distinctive malformation (MCA/MR) syndrome in which the phenotype correlates with the amount of chromosome material missing and which differs from the more variable phenotype associated with interstitial deletions of 4q.

Abnormalities, Multiple↗

Urinary tract involvement in EEC syndrome.

A patient with fully expressed, sporadic ectrodactyly, ectodermal dysplasia, and cleft lip and/or palate (EEC) syndrome with renal involvement is presented; descriptions of four similar patients were found in the literature. Based on these patients, we suggest that the renal involvement is a form of dysplasia secondary to fetal urinary tract obstruction. We emphasize the importance of searching for a urinary tract anomaly in patients with this uncommon syndrome.

Abnormalities, Multiple↗

[Moya-moya disease. Raynaud's phenomenon. IgA deficiency].

The authors report one case of Moya-Moya disease in a 3 month-old infant, who developed microcephaly, mental retardation and tetraparesis. The appearance in the following months of a Raynaud's phenomenon in the upper limbs and of IgA deficiency may be of interest for the understanding of the disease.

Arterial Occlusive Diseases↗

Swedish socialism and big business.

It is argued that during 44 years of Social Democratic government in Sweden intimate cooperation has developed between this government and multinational corporations. This cooperation was based upon the development of common interests, and was the result of an economic policy of structural rationalization and state intervention. A strong tendency of concentration of capital can be observed. Data are presented to support the theses developed.

Commerce↗