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. Author manuscript; available in PMC: 2020 Apr 1.
Published in final edited form as: Am J Med Genet A. 2019 Feb 4;179(4):542–551. doi: 10.1002/ajmg.a.61062

Table 2:

Clinical Features of Patients with Sotos Syndrome and HI

Patient 1 Patient 2 Patient 3 Patient 4ss Patient 5 Patient 6 Patient 7 Totals
Gender Female Female Male Male Male Female Male
Clinical Features
Central nervous system
Hypotonia + + + + 4/7
Other Tethered cord; seizures; prominent supratentorial ventricles; diffuse thinning of corpus callosum Diffuse thinning of corpus callosum; moderate to severe delays in myelination; ventriculomegaly Periventricular leukomalacia Abnormal EEG (background dyssyncrhony)
Cardiology
Cardiac defect - PDA; small PFO vs ASD LV enlargement PDA; small PFO vs ASD VSD PDA; ASD - 5/7
Genitourinary
- Pelvicaliectasis - Hydroceles (bilaterally) - - - 2/7
Other clinical features
Sacrococcygeal teratoma; scoliosis Sacrococcygeal teratoma; obstructive sleep apnea Metopic craniosynostosis Congenital kyphosis; umbilical hernia - Bronchopulmonary dysplasia; recurrent aspiration pneumonia; hiatal hernia -
Atypical features
Failure to thrive; Sacrococcygeal teratoma Sacrococcygeal teratoma Metopic craniosynostosis Failure to thrive

EEG- electroencephalogram; PDA- patent ductus arteriosis; PFO- patent foramen ovale; ASD- atrial septal defect; VES- ventricular septal defect