Wormian bone-multiple fractures-dentinogenesis imperfecta-skeletal dysplasia

Skeletal dysplasia with wormian bone-multiple fractures-dentinogenesis imperfecta is a skeletal disorder, reported in three patients to date, characterized clinically by multiple fractures, wormian bones of the skull, dentinogenesis imperfecta and facial dysmorphism (hypertelorism, periorbital fullness). Although the signs are very similar to osteogenesis imperfecta, characteristic cortical defects in the absence of osteopenia and collagen abnormalities are considered to be distinctive. There have been no further descriptions in the literature since 1999.



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Matched Phenotype  Gene  Mutation  MeSH
Rank
(Similarity)
PMID
(PMCID)
        

Phenotype(s) retrieved from Orphanet

    Total: 13

HPO ID Term Frequency
HP:0000703 Dentinogenesis imperfecta Very frequent (99-80%)
HP:0011120 Concave nasal ridge Very frequent (99-80%)
HP:0000268 Dolichocephaly Frequent (79-30%)
HP:0000316 Hypertelorism Frequent (79-30%)
HP:0000629 Periorbital fullness Frequent (79-30%)
HP:0002645 Wormian bones Frequent (79-30%)
HP:0002756 Pathologic fracture Frequent (79-30%)
HP:0003103 Abnormal cortical bone morphology Frequent (79-30%)
HP:0004322 Short stature Frequent (79-30%)
HP:0009824 Upper limb undergrowth Frequent (79-30%)
HP:0001376 Limitation of joint mobility Occasional (29-5%)
HP:0001773 Short foot Occasional (29-5%)
HP:0001863 Toe clinodactyly Occasional (29-5%)


Phenotype(s) retrieved from case reports

    Total: 0

HPO ID Term # of case reports


Causative gene(s) retrieved from Orphanet

    Total: 0

Gene Symbol Gene Name Entrez Gene ID