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Published in 2018 at "Acta Neurologica Scandinavica"
DOI: 10.1111/ane.13006
Abstract: Monosomy 1p36 syndrome is a recognized syndrome with multiple congenital anomalies; medical problems of this syndrome include developmental delay, facial dysmorphisms, hearing loss, short stature, brain anomalies, congenital heart defects. Epilepsy can be another feature…
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Keywords:
epilepsy monosomy;
1p36 syndrome;
syndrome implications;
features epilepsy ... See more keywords