lissencephaly type 3-metacarpal bone dysplasia syndrome https://www.malacards.org/card/lissencephaly_type_3_metacarpal_bone_dysplasia_syndrome https://www.malacards.org/card/lissencephaly_type_iii_and_bone_dysplasia GARD:0016763 lissencephaly type 3 and bone dysplasia lissencephaly type III and bone dysplasia This syndrome is characterized by severe microcephaly, agyria, agenesis of the corpus callosum, cerebellar hypoplasia, facial dysmorphology and epiphyseal stippling of the metacarpal bones. It has been described in two brothers. The syndrome is transmitted as an autosomal recessive trait and may be an allelic variant of Neu-Laxova syndrome and Lissencephaly type III with cystic dilations of the cerebellum and fetal akinesia sequence. Orphanet:86822 MONDO:0011004 UMLS:C1832678 MESH:C563383 SCTID:718720007 MEDGEN:371379 OMIM:601160 lissencephaly type 3