Electroclinical features of epilepsy monosomy 1p36 syndrome and their implications
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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… read more here.
Keywords: epilepsy monosomy; 1p36 syndrome; syndrome implications; features epilepsy ... See more keywords