By H. Galjaard, H.F.R. Prechtl, M. Velickovic

At the top of September 1984 Dr. M. Velickovi~ and Prof. H. Prechtl with assistance from the foreign Cerebral Palsy Society prepared a world convention on "New boost­ ments within the evaluate of early mind harm" in Bled, Yugo­ slavia. i used to be invited as a speaker at this convention and that i went there, curious, yet with out an excessive amount of wisdom in regards to the valuable topic: cerebral palsy. throughout the convention and a satellite tv for pc assembly I turned inspired by way of the standard of varied contributions and in addition through the nice number of difficulties regarding the etiology, early analysis, administration and psychosocial features of cerebral palsy. this present day, in lots of components of biology and medication, development turns out to require focus on a truly slim box. in this case many meetings are hugely really expert and so much (young) scientists rightly ponder this as most respected for his or her personal paintings. nonetheless the care of sufferers and counselling of oldsters and different shut family require a multidisciplinary procedure. additionally, advances within the learn of complex un­ resolved scientific organic pr'oblems are usually made unex­ pectedly by utilizing principles, theories, methods or equipment from different disciplines.

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Clinics in Developmental Medicine No 87. Stanley F, Alberman A (Eds). Spastics International Medical Publications, 116-34, Oxford. Hagberg B, Hagberg G (1985): Role of perinatal asphyxia hypoxia in the epidemiology of brain damage. Review. 4th International Berlin Symposium on Infant Mortality. Berlin GDR, September 22-26, 1985. Hagberg B (1985): Hypoxic and traumatic brain injury at term. Review. lOth Annual Perinatal Meeting of The British Association of Perinatal Paediatrics, Dundee, July 20, 1985.

York. 27. WHO reports on the Comments Control of Hereditary Anemias (1983 a,b), WHO Geneva. 28. Ku1iev A, Modell Band Ga1jaard H (1985): Perspectives in fetal diagnosis of congenital disorders, WHO/Serono Symposium, Serono Symp Reviews, Rome. 29. Emery AEH and Rimoin DL (1983): Principles and practice of medical genetics, Vo1s 1 and 2, Churchill Livingstone, Edingburgh. 30. Bickel H and Guthrie Rand Hammersen G (eds) (1980): Neonatal screening for inborn errors of metabolism, Springer, Berlin. 31.

32 - syndromes associated with chromosome breakage such as Bloom syndrome or Fanconi anemia. - possible carriership of a balanced chromosome translocation because of the presence of a hereditary chromosome anomaly in one or more relative{s). - recurrent ~2) spontaneous abortions because in these instances 5-10% of one of the parents is a carrier of a balanced chromosome translocation or another chromosome anomaly (22). A special category of indications are the leucemias and other myeloproliferative disorders where chromosome analysis of bone marrow cells may be important for an exact classification of the disease and for the prognosis and treatment.

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