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Biomedical subjects

V A Morgan

Publications and source records attributed to V A Morgan.

5 recordsLinked to original sources

Season of birth in schizophrenia and affective psychoses in Western Australia 1916-61.

OBJECTIVE: This study examines seasonality birth effects in schizophrenia and affective psychoses in the southern hemisphere, given possible confounding of age-incidence effects with winter birth peaks in northern hemisphere data. METHOD: Distributions of births by season, quarter and month for individuals born in Western Australia 1916-61 with a diagnosis of schizophrenia (N=2284), affective psychoses (N=3236), and neurotic depression (N=4869) on the statewide mental health register were compared with distributions for the general population. RESULTS: We found no association between season of birth and schizophrenia, affective psychoses or neurotic depression. For schizophrenia, the pattern of risks by quarter reflects northern hemisphere trends. Results by month are difficult to interpret due to large fluctuations in the data. While age-incidence effects had no impact on the distribution of risk, we found an artefactual increase in January births due to routine imputation of missing birth dates. CONCLUSION: Adjusting for artefacts in the data produced a pattern analogous to northern hemisphere trends.

Adult↗

1,6-hexanediol diacrylate: a rapid and potent sensitizer in the printing industry.

Printers are exposed to a wide variety of irritants and sensitizers. Allergy developing from a single exposure to any compound is rare. We report two cases of workers in the printing industry who developed allergic contact dermatitis to 1,6-hexanediol diacrylate (HDDA) within a short period of exposure. The first developed within weeks of exposure to a plastic sheet primed with HDDA. The second developed after a single accidental exposure.

Accidents, Occupational↗

A case of spontaneous mutation in the keratin 9 gene associated with epidermolytic palmoplantar keratoderma.

Epidermolytic palmoplantar keratoderma appears to be due to defects in keratin 9, the palmoplantar specific type 1 keratin. We report a case of spontaneous mutation, a C to T transition at codon 162, resulting in an arginine to tryptophan substitution in the 1 A region of the alpha helical rod domain of keratin 9. This provides further evidence that this codon is an important spot for mutation in keratin 9.

Child, Preschool↗

Skin disease in general practice.

Out of 336 consultations in general practice 52 (15%) concerned a dermatological problem. Sun related problems, eczema/dermatitis and infection were encountered most frequently.

Adolescent↗