Table 1 Additional phenotypes of patients with syndromic obesity
From: Chromosomal microarray analysis in the genetic evaluation of 279 patients with syndromic obesity
| Clinical features | Total cohort (n) | Patients with PCNVs (n) |
|---|---|---|
| Intellectual/developmental disabilities | 219 | 55 |
| Craniofacial dysmorphism | 149 | 49 |
| Behavioral problems | 132 | 29 |
| Hyperphagia | 112 | 27 |
| Infantile hypotonia | 88 | 32 |
| Language impairments | 80 | 28 |
| Hands/ft abnormalities | 65 | 21 |
| Abnormal external genitalia | 56 | 20 |
| Eye/vision problems | 51 | 16 |
| Seizures | 31 | 13 |
| Poor motor skills | 29 | 9 |
| Skeletal anomalies | 23 | 9 |
| Brain abnormalities | 19 | 7 |
| Hearing loss | 13 | 6 |
| Cardiac abnormalities | 10 | 4 |