Microcephaly in Australian infants: A retrospective audit.
Carlos NunezAnne MorrisMichele HansenElizabeth J ElliottPublished in: Journal of paediatrics and child health (2021)
Our results suggest the need for a systematic investigative approach to diagnosis, including a careful history, examination, genetic testing and neuroimaging, to determine the underlying cause of microcephaly, identify co-morbidities, predict prognosis and guide genetic counselling and therapy.