Low nose bridge

The nasal bridge is the name given to the upper, bony part of the nose, overlying the nasal bones. A lower or higher than average nasal bridge can be a sign of various genetic disorders.

• 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

• 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

• 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)