Category
page 1Syndromes affecting teeth
Williams-Beuren syndrome
neurodevelopmental disorder caused by a deletion of around 27 genes in chromosome 7, characterized by a broad forehead, underdeveloped chin, short nose, full cheeks, challenges with visual tasks, increased empathy and decreased aggression
DiGeorge syndrome
T cell deficiency disease that is the result of a large deletion of chromosome 22, which includes the DGS gene needed for development of the thymus and related glands with subsequent lack of T-cell production
amelogenesis imperfecta
dental enamel hypoplasia characterized by abnormal enamel formation
Ellis–Van Creveld syndrome
Human disease
ectodermal dysplasia
human disease
Meige syndrome
cranio-facial dystonia that is accompanied by blepharospasm
ectrodactyly–ectodermal dysplasia–cleft syndrome
autosomal dominant disease characterized by ectrodactyly, ectodermal dysplasia, and orofacial clefts (cleft lip-palate)
oral-facial-digital syndrome
genetic disease that is characterized by malformations of the face, oral cavity, and digits with polycystic kidney disease and variable involvement of the central nervous system and has material basis in X-linked inheritance of an OFD gene
trichorhinophalangeal syndrome type II
Human disease
Papillon-Lefevre disease
Human disease
Haim–Munk syndrome
Haim-Munk syndrome (HMS) is characterized by palmoplantar hyperkeratosis, severe early-onset periodontitis, onychogryposis, pes planus, arachnodactyly and acroosteolysis
Kohlschütter-Tönz syndrome
rare inherited human disease
Nance-Horan syndrome
disorder of lens
Ackerman syndrome
medical condition
tricho–dento–osseous syndrome
congenital disorder of digestive system