Rett syndrome

Journal of Medical Genetics

Volumn 33, Issue 8, 1996, Pages 693-699

  Clarke, Angus ^a  

^a CARDIFF UNIVERSITY   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ORNITHINE CARBAMOYLTRANSFERASE;

CLINICAL FEATURE; CYTOGENETICS; DIFFERENTIAL DIAGNOSIS; FEMALE; HUMAN; HYPERAMMONEMIA; INHERITANCE; NEUROCHEMISTRY; NEUROPATHOLOGY; PRIORITY JOURNAL; RETT SYNDROME; SHORT SURVEY; UREA CYCLE; X CHROMOSOME LINKAGE;

EID: 0029760340     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: 10.1136/jmg.33.8.693     Document Type: Short Survey

References (14)

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3. Rett A. Cerebral atrophy associated with hyperammonaemia. In: Vinken PJ, Bruyn GW, in association with Klawans HL, eds. Metabolic and deficiency diseases of the nervous system III. Chapter 16. Handbook of Clinical Neurology Volume 26. Amsterdam: Elsevier/North Holland Biomedical Press, 1977.
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11. Witt-Engerstrom I. Rett syndrome: the late infantile regression period - a retrospective analysis of 91 cases. Acta Paediatr 1992;81:167-72.
12. Witt-Engerstrom I. Rett syndrome: a retrospective pilot study on potential early predictive symptomatology. Brain Dev 1987;9:481-6.
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14. The Rett Syndrome Diagnostic Criteria Working Group. Diagnostic criteria for Rett syndrome. Ann Neurol 1988;23:425-8.