Developmental and genetic diseases
Atlas of developmental and genetic dental diseases
- Acrocallosal syndrome
- Acroosteolysis with osteoporosis and changes in skull and mandible
- ADULT syndrome
- Amelogenesis imperfecta
- Amelogenesis imperfecta, hypoplastic/hypomaturation, X-linked 1
- Amelogenesis imperfecta, hypoplastic type, IG
- Amelogenesis imperfecta 1, hypoplastic type
- Amelogenesis imperfecta 2, hypoplastic local, autosomal dominant
- Amelogenesis imperfecta, pigmented hypomaturation type
- Amelogenesis imperfecta, type IB
- Amelogenesis imperfecta, type IC
- Anauxetic dysplasia
- Apert syndrome - Dental anomalies
- Axenfeld-Rieger syndrome, type 1
- Brittle cornea syndrome
- Burkitt lymphoma
- Cherubism - Dental anomalies
- Cleft lip / cleft palate - Dental anomalies
- Cleidocranial dysplasia - Dental anomalies
- Cornelia de Lange syndrome
- Cowden disease - Dental anomalies
- Crouzon syndrome
- Cytomegalovirus infection, congenital
- Deafness, congenital, with inner ear agenesis, microtia, and microdontia
- Dens invaginatus
- Dental ectopia
- Dental transposition
- Dentin dysplasia, type I
- Dentin dysplasia, type II
- Dentinogenesis imperfecta
- Dentinogenesis imperfecta 1
- Dubowitz syndrome
- Duchenne muscular dystrophy
- Ectodermal dysplasia, hypohidrotic, autosomal dominant
- Ectodermal dysplasia, hypohidrotic, autosomal recessive
- Ectodermal dysplasia, hypohidrotic, with immune deficiency
- Ectodermal dysplasia, hypohidrotic, X-linked - Dental anomalies
- EEC syndrome
- EEM syndrome
- Ellis-van Creveld syndrome - Dental anomalies
- Epidermolysis bullosa, junctional, non-Herlitz type
- Fibromatosis, gingival
- Fibromatosis, gingival, 1
- Frontonasal dysplasia
- GAPO syndrome
- Glanzmann thrombasthenia - Dental anomalies
- Goldenhar syndrome - Dental anomalies
- Gorlin syndrome
- Griscelli syndrome - Dental anomalies
- Haim-Munk syndrome
- Hay-Wells syndrome
- Hyalinosis, infantile systemic
- Hyperdontia
- Hypodontia
- Hypophosphatasia
- Hypophosphatasia, infantile
- Incontinentia pigmenti
- Kabuki syndrome
- Klippel-Trenaunay-Weber syndrome
- Laugier-Hunziker syndrome
- Marfan syndrome
- Microphthalmia, syndromic 2
- Naegeli-Franceschetti-Jadassohn syndrome
- Nance-Horan syndrome
- Noonan syndrome
- Oculodentodigital dysplasia
- Oligodontia
- Oligodontia-colorectal cancer syndrome
- Osteogenesis imperfecta
- Osteopetrosis, autosomal recessive
- Papillon-Lefevre syndrome - Dental anomalies
- Parry-Romberg syndrome
- Porphyria cutanea tarda
- Primary failure of eruption
- Pseudohypoparathyroidism, type Ia
- Pyknodysostosis
- Pyle disease
- Regional odontodysplasia
- Robinow syndrome
- Sickle cell anemia - Dental anomalies
- Split-hand/foot malformation with sensorineural hearing loss
- Sturge-Weber syndrome - Dental anomalies
- Syngnathia
- Syphilis, congenital
- Talon cusp
- Teeth present at birth
- Tooth agenesis, selective, 1
- Tooth agenesis, selective, 2
- Tooth agenesis, selective, 3
- Treacher Collins syndrome
- Trichodentoosseous syndrome
- Trichorhinophalangeal syndrome, type I
- Trisomy 21 - Dental anomalies
- Tuberous sclerosis - Dental anomalies
- Van der Woude syndrome
- Walker-Warburg syndrome
- White sponge nevus of Cannon
- Williams-Beuren syndrome
- Witkop syndrome
- Wolf-Hirschhorn syndrome
- Xanthinuria, type II
Edited by Aldo Campana,