Micrognathism: Difference between revisions
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==Causes== | ==Causes== | ||
*49,XXXXX syndrome | *[[49,XXXXX syndrome]] | ||
*Atkin-Flaitz-Patil syndrome | *[[Atkin-Flaitz-Patil syndrome]] | ||
*Bowen-Conradi syndrome | *[[Bowen-Conradi syndrome]] | ||
*Camptomelic dysplasia | *[[Camptomelic dysplasia]] | ||
*Cardiofaciocutaneous | *[[Cardiofaciocutaneous syndrome]] | ||
*Carey-Fineman-Ziter syndrome | *[[Carey-Fineman-Ziter syndrome]] | ||
*Catel-Manzke syndrome | *[[Catel-Manzke syndrome]] | ||
*Cerebrocostomandibular syndrome | *[[Cerebrocostomandibular syndrome]] | ||
*Cerebrohepatorenal syndrome | *[[Cerebrohepatorenal syndrome]] | ||
*CHARGE syndrome | *[[CHARGE syndrome]] | ||
*Chromosome 18 trisomy syndrome | *[[Chromosome 18 trisomy syndrome]] | ||
*Chromosome 8 recombinant syndrome | *[[Chromosome 8 recombinant syndrome]] | ||
*Chromosome 8 trisomy syndrome | *[[Chromosome 8 trisomy syndrome]] | ||
*CODAS (cerebral, ocular, dental, auricular, skeletal) syndrome | *[[CODAS (cerebral, ocular, dental, auricular, skeletal) syndrome]] | ||
*Coffin-Lowry syndrome | *[[Coffin-Lowry syndrome]] | ||
*Cohen syndrome | *[[Cohen syndrome]] | ||
*Cornelia de Lange syndrome | *[[Cornelia de Lange syndrome]] | ||
*Craniomandibular dermatodysostosis | *[[Craniomandibular dermatodysostosis]] | ||
*Cri du chat syndrome 5p− | *[[Cri du chat syndrome 5p−]] | ||
*De la Chapelle dysplasia | *[[De la Chapelle dysplasia]] | ||
*Diamond-Blackfan anemia | *[[Diamond-Blackfan anemia]] | ||
*DiGeorge's syndrome | *[[DiGeorge's syndrome]] | ||
*Dubowitz syndrome | *[[Dubowitz syndrome]] | ||
*Femoral hypoplasia - unusual facies syndrome | *[[Femoral hypoplasia - unusual facies syndrome]] | ||
*Fetal akinesia-hypokinesia sequence | *[[Fetal akinesia-hypokinesia sequence]] | ||
*Fetal aminopterin-like syndrome | *[[Fetal aminopterin-like syndrome]] | ||
*Hurst's microtia-absent patellae-micrognathia syndrome | *[[Hurst's microtia-absent patellae-micrognathia syndrome]] | ||
*Juvenile chronic arthritis | *[[Juvenile chronic arthritis]] | ||
*Kyphomelic dysplasia | *[[Kyphomelic dysplasia]] | ||
*Lathosterolosis | *[[Lathosterolosis]] | ||
*Lethal congenital contracture syndrome | *[[Lethal congenital contracture syndrome]] | ||
*Lethal restrictive dermopathy | *[[Lethal restrictive dermopathy]] | ||
*Loeys-Dietz syndrome | *[[Loeys-Dietz syndrome]] | ||
*Lujan-Fryns syndrome | *[[Lujan-Fryns syndrome]] | ||
*Marden-Walker syndrome | *[[Marden-Walker syndrome]] | ||
*Marfan's syndrome | *[[Marfan's syndrome]] | ||
*Micrognathia with peromelia | *[[Micrognathia with peromelia]] | ||
*Miller-Dieker syndrome | *[[Miller-Dieker syndrome]] | ||
*Nager acrofacial dysostosis | *[[Nager acrofacial dysostosis]] | ||
*Noonan's syndrome | *[[Noonan's syndrome]] | ||
*Opitz-Frias syndrome | *[[Opitz-Frias syndrome]] | ||
*Orofaciodigital syndrome type 4 | *[[Orofaciodigital syndrome type 4]] | ||
*Otopalatodigital syndrome type 2 | *[[Otopalatodigital syndrome type 2]] | ||
*Pallister-Hall syndrome | *[[Pallister-Hall syndrome]] | ||
*Pierre Robin syndrome | *[[Pierre Robin syndrome]] | ||
*Postaxial acrofacial dysostosis syndrome | *[[Postaxial acrofacial dysostosis syndrome]] | ||
*Rothmund-Thomson syndrome | *[[Rothmund-Thomson syndrome]] | ||
*Schwartz-Jampel-Aberfeld syndrome | *[[Schwartz-Jampel-Aberfeld syndrome]] | ||
*Scott craniodigital syndrome | *[[Scott craniodigital syndrome]] | ||
*Smith-Lemli-Opitz syndrome | *[[Smith-Lemli-Opitz syndrome]] | ||
*Syphilis, congenital | *[[Syphilis, congenital]] | ||
*Ter Haar syndrome | *[[Ter Haar syndrome]] | ||
*Toriello-Carey syndrome | *[[Toriello-Carey syndrome]] | ||
*Treacher Collins-Franceschetti syndrome | *[[Treacher Collins-Franceschetti syndrome]] | ||
*Trichorhinophalangeal syndrome type 1 | *[[Trichorhinophalangeal syndrome type 1]] | ||
*Trichorhinophalangeal syndrome type 3 | *[[Trichorhinophalangeal syndrome type 3]] | ||
*Turner's syndrome | *[[Turner's syndrome]] | ||
*Van Bogaert-Hozay syndrome | *[[Van Bogaert-Hozay syndrome]] | ||
*Wagner vitreoretinal degeneration syndrome | *[[Wagner vitreoretinal degeneration syndrome]] | ||
*Weissenbacher-Zweymuller syndrome | *[[Weissenbacher-Zweymuller syndrome]] | ||
*Wolf-Hirschhorn syndrome | *[[Wolf-Hirschhorn syndrome]] | ||
*Yunis-Varon syndrome | *[[Yunis-Varon syndrome]] | ||
Its causes also include , | Its causes also include , , [[Hallerman-Streiff syndrome]], [[Trisomy 13]], [[Trisomy 18]], X0 syndrome ([[Turner syndrome]]), [[Progeria]], [[Treacher Collins syndrome]], [[Smith-Lemli-Opitz syndrome]], [[Russell-Silver syndrome]], [[Seckel syndrome]], [[Cri du chat syndrome]] and [[Marfan syndrome]]. | ||
==Diagnosis== | ==Diagnosis== | ||
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==See also== | ==See also== | ||
* [[Mandible]] | *[[[[Mandible]] | ||
==References== | ==References== | ||
Revision as of 23:12, 29 July 2012
| Micrognathism | |
| ICD-10 | K07.0 |
|---|---|
| ICD-9 | 524.04 |
| DiseasesDB | 22641 |
| MedlinePlus | 003306 |
| MeSH | D008844 |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
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Synonyms and keywords: Micrognathia, mandibular hypoplasia
Overview
Micrognathism is a condition where the jaw is undersized.
Natural History, Complications, Prognosis
It is common in infants, but is usually self-corrected during growth, due to the jaws increasing in size.
It may be a cause of abnormal tooth alignment and in severe cases can cause hamper feeding.
Causes
Its causes also include , , Hallerman-Streiff syndrome, Trisomy 13, Trisomy 18, X0 syndrome (Turner syndrome), Progeria, Treacher Collins syndrome, Smith-Lemli-Opitz syndrome, Russell-Silver syndrome, Seckel syndrome, Cri du chat syndrome and Marfan syndrome.
Diagnosis
Skull X ray
It can be detected by dental or skull X-Ray testing.
See also
- [[Mandible