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. 2014 Jul 20;8(7):ZD28–ZD30. doi: 10.7860/JCDR/2014/8842.4608

[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