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. 2022 Jan 16;30(3):384–388. doi: 10.1038/s41431-021-01023-4

Table 1.

The reported clinical features of bi-allelic or recessive SMO cases [7, 8].

Le et al. [8] This report
F1-II:1 F2-II:1a F2-II:2a F3-II:1 F4-II:4 F5-II:2 F5-II:3 II-1 II-2
Sex M M M M M M F M F
Psychomotor development normal normal normal mild delay normal NR normal severe delay mild delay
Gelastic seizures + + + + +
Hypothalamic hamartoma + + + NR NR + +
Microcephaly + + +
Dysmorphic facial features + + + + +
Chest and rib abnormalities + moderate
Postaxial polydactyly + + + + + + + + +
Syndactyly 5/6 2/3 5/6 2/3 2/3 3/4
Cardiac defect + + +
Shortening of long bones + + +

We report two cases (II-1 & II-2) that share the clinical features of hypothalamic hamartoma, gelastic seizures, developmental delay, microcephaly (<3rd centile), post-axial polydactyly and shortening of the long bones. The male proband (II-1) had precocious puberty and hypospadias.

NR not reported.

aPreviously reported [7].