Dentinogenesis imperfecta-short stature-hearing loss-intellectual disability syndrome

Orpha code: 71267OMIM code:

Definition

A rare malformative syndrome with dentinogenesis imperfecta, characterized by dentin dysplasia with opalescent discoloration and severe attrition of primary and permanent teeth, and delayed eruption, bulbous crowns, long and tapered roots, and progressive root canal obliteration of the permanent dentition, associated with proportionate short stature, sensorineural hearing loss, mild intellectual disability, and dysmorphic facial features. The latter include a prominent nose with high nasal bridge and short philtrum. Osteoporosis, mild platyspondyly, and cone-shaped epiphyses have also been reported.

Disease data
Classification

Malformation syndrome

Synonyms
Dentinogenesis imperfecta-short stature-deafness-intellectual disability syndrome
Dentinogenesis imperfecta-short stature-deafness-intellectual disability syndrome
ORPHA code
71267
OMIM code
-
ICD10 code
-
ICD11 code
-

No additional description.

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