Low nose bridge: Difference between revisions
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==Causes== | ==Causes== | ||
===Causes In Alphabetical Order=== | ===Causes In Alphabetical Order=== | ||
*[[18p | *[[18p minus syndrome]] | ||
*[[49,XXXXX | *[[49,XXXXX syndrome]] | ||
*[[49,XXXXY | *[[49,XXXXY syndrome]] | ||
*[[Achondrogenesis | *[[Achondrogenesis type 1A and 1B]] | ||
*[[Achondrogenesis | *[[Achondrogenesis type 1B]] | ||
*[[Acrodysostosis ]] | *[[Acrodysostosis ]] | ||
*[[Albright's | *[[Albright's hereditary osteodystrophy]] | ||
*[[Blepharophimosis, | *[[Blepharophimosis, ptosis, epicanthus inversus]] | ||
*[[Campomelic | *[[Campomelic dysplasia]] | ||
*[[Chondrodysplasia | *[[Chondrodysplasia Punctata, Rhizomelic type]] | ||
*[[Chromosome | *[[Chromosome 18, Monosomy 18p]] | ||
*[[Chromosome | *[[Chromosome 18p minus syndrome]] | ||
*[[Chromosome | *[[Chromosome 19p duplication syndrome]] | ||
*[[Chromosome | *[[Chromosome 20, deletion 20p]] | ||
*[[Chromosome | *[[Chromosome 20p deletion syndrome]] | ||
*[[Chromosome | *[[Chromosome 8, trisomy 8p]] | ||
*[[Chromosome | *[[Chromosome 8p duplication syndrome]] | ||
*[[Cleidocranial | *[[Cleidocranial dysplasia]] | ||
*[[Conradi-Hunermann | *[[Conradi-Hunermann syndrome]] | ||
*[[Conradi-Hünermann | *[[Conradi-Hünermann Syndrome]] | ||
*[[Deletion 20p]] | *[[Deletion 20p]] | ||
*[[Duplication | *[[Duplication 8p]] | ||
*[[Ectodermal | *[[Ectodermal dysplasia, hypohidrotic, autosomal dominant]] | ||
*[[Ectodermal | *[[Ectodermal dysplasia, hypohidrotic, autosomal recessive]] | ||
*[[German | *[[German syndrome]] | ||
*[[Hurler | *[[Hurler syndrome]] | ||
*[[I cell | *[[I cell disease]] | ||
*[[Kniest | *[[Kniest dysplasia]] | ||
*[[Marshall-Smith | *[[Marshall-Smith Syndrome]] | ||
*[[Monosomy 20p]] | *[[Monosomy 20p]] | ||
*[[Mucopolysaccharidosis | *[[Mucopolysaccharidosis type 6]] | ||
*[[Mucopolysaccharidosis | *[[Mucopolysaccharidosis type I Hurler syndrome]] | ||
*[[Mucopolysaccharidosis | *[[Mucopolysaccharidosis type I Hurler-Scheie syndrome]] | ||
*[[Neurofibromatosis-Noonan | *[[Neurofibromatosis-Noonan syndrome]] | ||
*[[Noonan | *[[Noonan Syndrome]] | ||
*[[Osteogenesis | *[[Osteogenesis imperfecta type II]] | ||
*[[Osteogenesis | *[[Osteogenesis imperfecta, type 2]] | ||
*[[Osteogenesis | *[[Osteogenesis imperfecta, type 2A]] | ||
*[[Osteogenesis | *[[Osteogenesis imperfecta, type IIB]] | ||
*[[Pfeiffer | *[[Pfeiffer syndrome Type 1]] | ||
*[[Rapp-Hodgkin | *[[Rapp-Hodgkin syndrome]] | ||
*[[Rhizomelic | *[[Rhizomelic chondrodysplasia punctata, type 1]] | ||
*[[Rhizomelic | *[[Rhizomelic chondrodysplasia punctata, type 3]] | ||
*[[Schinzel | *[[Schinzel Giedion Syndrome]] | ||
*[[Thanatophoric | *[[Thanatophoric dysplasia]] | ||
*[[Thanatophoric | *[[Thanatophoric dysplasia, type 1]] | ||
*[[Thanatophoric | *[[Thanatophoric dysplasia, type 2]] | ||
*[[Triploid | *[[Triploid syndrome]] | ||
*[[Valproic | *[[Valproic acid antenatal infection]] | ||
*[[Walker-Warburg | *[[Walker-Warburg Syndrome]] | ||
*[[X-linked | *[[X-linked alpha thalassemia mental retardation syndrome (ATR-X)]] |
Revision as of 00:07, 30 July 2012
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Synonyms and keywords: low nasal bridge