Low nose bridge: Difference between revisions

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{{SK}} low nasal bridge


==Overview==
==Overview==
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==Causes==
==Causes==
===Causes In Alphabetical Order===
===Causes In Alphabetical Order===
18p  minus syndrome
*[[18p  minus syndrome


49,XXXXX  syndrome
*[[49,XXXXX  syndrome


49,XXXXY  syndrome
*[[49,XXXXY  syndrome


Achondrogenesis  type 1A and 1B
*[[Achondrogenesis  type 1A and 1B


Achondrogenesis  type 1B
*[[Achondrogenesis  type 1B


Acrodysostosis  
*[[Acrodysostosis  


Albright's  hereditary osteodystrophy
*[[Albright's  hereditary osteodystrophy


Blepharophimosis,  ptosis, epicanthus inversus
*[[Blepharophimosis,  ptosis, epicanthus inversus


Campomelic  dysplasia
*[[Campomelic  dysplasia


Chondrodysplasia  Punctata, Rhizomelic type
*[[Chondrodysplasia  Punctata, Rhizomelic type


Chromosome  18, Monosomy 18p
*[[Chromosome  18, Monosomy 18p


Chromosome  18p minus syndrome
*[[Chromosome  18p minus syndrome


Chromosome  19p duplication syndrome
*[[Chromosome  19p duplication syndrome


Chromosome  20, deletion 20p
*[[Chromosome  20, deletion 20p


Chromosome  20p deletion syndrome
*[[Chromosome  20p deletion syndrome


Chromosome  8, trisomy 8p
*[[Chromosome  8, trisomy 8p


Chromosome  8p duplication syndrome
*[[Chromosome  8p duplication syndrome


Cleidocranial  dysplasia
*[[Cleidocranial  dysplasia


Conradi-Hunermann  syndrome
*[[Conradi-Hunermann  syndrome


Conradi-Hünermann  Syndrome
*[[Conradi-Hünermann  Syndrome


Deletion 20p -  Low nasal bridge
*[[Deletion 20p -  Low nasal bridge


Duplication  8p
*[[Duplication  8p


Ectodermal  dysplasia, hypohidrotic, autosomal dominant
*[[Ectodermal  dysplasia, hypohidrotic, autosomal dominant


Ectodermal  dysplasia, hypohidrotic, autosomal recessive
*[[Ectodermal  dysplasia, hypohidrotic, autosomal recessive


German  syndrome
*[[German  syndrome


Hurler  syndrome
*[[Hurler  syndrome


I cell  disease
*[[I cell  disease


Kniest  dysplasia
*[[Kniest  dysplasia


Marshall-Smith  Syndrome
*[[Marshall-Smith  Syndrome


Monosomy 20p -  Low nasal bridge
*[[Monosomy 20p -  Low nasal bridge


Mucopolysaccharidosis  type 6
*[[Mucopolysaccharidosis  type 6


Mucopolysaccharidosis  type I Hurler syndrome
*[[Mucopolysaccharidosis  type I Hurler syndrome


Mucopolysaccharidosis  type I Hurler-Scheie syndrome
*[[Mucopolysaccharidosis  type I Hurler-Scheie syndrome]]


Neurofibromatosis-Noonan  syndrome
*[[Neurofibromatosis-Noonan  syndrome]]


Noonan  Syndrome
*[[Noonan  Syndrome]]


Osteogenesis  imperfecta type II
*[[Osteogenesis  imperfecta type II]]


Osteogenesis  imperfecta, type 2
*[[Osteogenesis  imperfecta, type 2]]


Osteogenesis  imperfecta, type 2A
*[[Osteogenesis  imperfecta, type 2A]]


Osteogenesis  imperfecta, type IIB
*[[Osteogenesis  imperfecta, type IIB]]


Pfeiffer  syndrome Type 1
*[[Pfeiffer  syndrome Type 1]]


Rapp-Hodgkin  syndrome
*[[Rapp-Hodgkin  syndrome]]


Rhizomelic  chondrodysplasia punctata, type 1
*[[Rhizomelic  chondrodysplasia punctata, type 1]]


Rhizomelic  chondrodysplasia punctata, type 3
*[[Rhizomelic  chondrodysplasia punctata, type 3]]


Schinzel  Giedion Syndrome
*[[Schinzel  Giedion Syndrome]]


Thanatophoric  dysplasia
*[[Thanatophoric  dysplasia]]


Thanatophoric  dysplasia, type 1
*[[Thanatophoric  dysplasia, type 1]]


Thanatophoric  dysplasia, type 2
*[[Thanatophoric  dysplasia, type 2]]


Triploid  syndrome
*[[Triploid  syndrome]]


Valproic  acid antenatal infection
*[[Valproic  acid antenatal infection]]


Walker-Warburg  Syndrome
*[[Walker-Warburg  Syndrome]]


X-linked  alpha thalassemia mental retardation syndrome (ATR-X)
*[[X-linked  alpha thalassemia mental retardation syndrome (ATR-X)]]

Revision as of 00:04, 30 July 2012

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

Synonyms and keywords: low nasal bridge

Overview

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