[Table/Fig-7]:
Comparison with syndromes and conditions constituting some (but not all) manifestations of present case
| Syndromes/ conditions | Skeletal features | Orofacial and Dental features |
| Taurodontism, microdontia and dens invaginatus [5] | Generalized microdontia, taurodontism of first permanent molars, multiple dens invaginatus | |
| Oculo-dento-digital dysplasia [11] | Bilateral micropthalmos, abnormally small nose, hypotrichosis, 5th finger camptodactyly, syndactyly of fourth and fifth fingers, missing toe phalanges | Enamel hypoplasia, thin dentinal walls, extensive caries, open apices |
| Symphalangism kantaputra type [5] | Distal symphalangism, hypoplastic carpal bones, brachydactyly, syndactyly of fingers and toes, cone shaped epiphyses, absent/small nails | Microdontia, dental pulp stones, narrowed zygomatic arch |
| Cranio ectodermal dysplasia [12] | Dolichocephaly, sparse slow growing fine hair, epicanthal folds, brachydactyly, narrow thorax | Hypodontia and/or microdontia |
| Trichodento-osseous syndrome [13] | Kinky curly hair, increased cranial thickness obliterated diploe and no visible mastoid pneumatization, thin brittle nails, dolichocephaly | Enamel hypoplasia, taurodontism |
| Russell silver syndrome [14] | Low birth weight, asymmetric growth of body, Clinodactyly, precocious puberty, short stature, Wide forehead with a small triangle-shaped face and small, narrow chin, café au lait birth marks, short arms fingers and toes | Mandibular micrognathia, deep bite, dental crowding, microdontia, high arched palate |