Low nose bridge: Difference between revisions
No edit summary |
No edit summary |
||
Line 1: | Line 1: | ||
{{SI}} | {{SI}} | ||
{{CMG}} | {{CMG}} | ||
{{SK}} low nasal bridge | |||
==Overview== | ==Overview== | ||
Line 6: | Line 8: | ||
==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
WikiDoc Resources for Low nose bridge |
Articles |
---|
Most recent articles on Low nose bridge Most cited articles on Low nose bridge |
Media |
Powerpoint slides on Low nose bridge |
Evidence Based Medicine |
Clinical Trials |
Ongoing Trials on Low nose bridge at Clinical Trials.gov Trial results on Low nose bridge Clinical Trials on Low nose bridge at Google
|
Guidelines / Policies / Govt |
US National Guidelines Clearinghouse on Low nose bridge NICE Guidance on Low nose bridge
|
Books |
News |
Commentary |
Definitions |
Patient Resources / Community |
Patient resources on Low nose bridge Discussion groups on Low nose bridge Patient Handouts on Low nose bridge Directions to Hospitals Treating Low nose bridge Risk calculators and risk factors for Low nose bridge
|
Healthcare Provider Resources |
Causes & Risk Factors for Low nose bridge |
Continuing Medical Education (CME) |
International |
|
Business |
Experimental / Informatics |
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