Histidinaemia: Study of Relation Between Clinical and Biological Findings in 7 Subjects
Open Access
- 1 April 1972
- journal article
- review article
- Published by BMJ in Archives of Disease in Childhood
- Vol. 47 (252) , 190-200
- https://doi.org/10.1136/adc.47.252.190
Abstract
Seven subjects with raised plasma histidine and low skin histidase levels (histidinaemia) are described: 4 were severely retarded, 2 showing in addition features of an early infantile psychosis (autism); 3 were of normal intelligence. There were no biochemical differences between the two groups. In view of these findings and a study of patients reported in the literature, attention is drawn to the difficulty in making a decision about treatment of a neonate detected by screening and shown to have the biochemical features of histidinaemia. The natural history of the condition is further examined, particularly the question of deterioration at time of seizures or infection.Keywords
This publication has 24 references indexed in Scilit:
- Maternal histidinaemia.Archives of Disease in Childhood, 1971
- DELAYED SPEECH AND HISTIDINAEMIADevelopmental Medicine and Child Neurology, 1970
- The simultaneous occurrence of histidinemia and congenital hypoplastic anemiaThe Journal of Pediatrics, 1969
- A SIMPLE ORAL TEST OF GROWTH-HORMONE SECRETION IN CHILDRENThe Lancet, 1968
- Histidinaemia: a child and his family.Archives of Disease in Childhood, 1968
- Biochemical and EEG studies in phenylketonuric children during phenylalanine tolerance testc.Archives of Disease in Childhood, 1966
- Further Case of HistidinaemiaBMJ, 1966
- A Case of HistidinaemiaArchives of Disease in Childhood, 1963
- Childhood PsychosisThe British Journal of Psychiatry, 1963
- HistidinemiaThe Journal of Pediatrics, 1962