Low nose bridge

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Causes

Causes In Alphabetical Order

18p minus syndrome

49,XXXXX syndrome

49,XXXXY syndrome

Achondrogenesis type 1A and 1B

Achondrogenesis type 1B

Acrodysostosis

Albright's hereditary osteodystrophy

Blepharophimosis, ptosis, epicanthus inversus

Campomelic dysplasia

Chondrodysplasia Punctata, Rhizomelic type

Chromosome 18, Monosomy 18p

Chromosome 18p minus syndrome

Chromosome 19p duplication syndrome

Chromosome 20, deletion 20p

Chromosome 20p deletion syndrome

Chromosome 8, trisomy 8p

Chromosome 8p duplication syndrome

Cleidocranial dysplasia

Conradi-Hunermann syndrome

Conradi-Hünermann Syndrome

Deletion 20p - Low nasal bridge

Duplication 8p

Ectodermal dysplasia, hypohidrotic, autosomal dominant

Ectodermal dysplasia, hypohidrotic, autosomal recessive

German syndrome

Hurler syndrome

I cell disease

Kniest dysplasia

Marshall-Smith Syndrome

Monosomy 20p - Low nasal bridge

Mucopolysaccharidosis type 6

Mucopolysaccharidosis type I Hurler syndrome

Mucopolysaccharidosis type I Hurler-Scheie syndrome

Neurofibromatosis-Noonan syndrome

Noonan Syndrome

Osteogenesis imperfecta type II

Osteogenesis imperfecta, type 2

Osteogenesis imperfecta, type 2A

Osteogenesis imperfecta, type IIB

Pfeiffer syndrome Type 1

Rapp-Hodgkin syndrome

Rhizomelic chondrodysplasia punctata, type 1

Rhizomelic chondrodysplasia punctata, type 3

Schinzel Giedion Syndrome

Thanatophoric dysplasia

Thanatophoric dysplasia, type 1

Thanatophoric dysplasia, type 2

Triploid syndrome

Valproic acid antenatal infection

Walker-Warburg Syndrome

X-linked alpha thalassemia mental retardation syndrome (ATR-X)