Micrognathism: Difference between revisions
No edit summary |
|||
| (6 intermediate revisions by the same user not shown) | |||
| Line 1: | Line 1: | ||
{{Infobox_Disease | | {{Infobox_Disease | | ||
Name = Micrognathism | | |||
Image = | | |||
Caption = | | |||
DiseasesDB = 22641 | | |||
ICD10 = {{ICD10|K|07|0|k|00}} | | |||
ICD9 = {{ICD9|524.04}} | | |||
ICDO = | | |||
OMIM = | | |||
MedlinePlus = 003306 | | |||
eMedicineSubj = | | |||
eMedicineTopic = | | |||
MeshID = D008844 | | |||
}} | }} | ||
{{CMG}} | {{CMG}} | ||
| Line 23: | Line 23: | ||
It is common in infants, but is usually self-corrected during growth, due to the jaws increasing in size. | 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 | It may be a cause of abnormal tooth alignment and in severe cases can cause hamper feeding. | ||
== | ==Causes== | ||
* [[ | *[[49,XXXXX syndrome]] | ||
== | *[[Atkin-Flaitz-Patil syndrome]] | ||
*[[Bowen-Conradi syndrome]] | |||
*[[Camptomelic dysplasia]] | |||
*[[Cardiofaciocutaneous syndrome]] | |||
*[[Carey-Fineman-Ziter syndrome]] | |||
*[[Catel-Manzke syndrome]] | |||
*[[Cerebrocostomandibular syndrome]] | |||
*[[Cerebrohepatorenal syndrome]] | |||
*[[CHARGE syndrome]] | |||
*[[Chromosome 18 trisomy syndrome]] | |||
*[[Chromosome 8 recombinant syndrome]] | |||
*[[Chromosome 8 trisomy syndrome]] | |||
*[[CODAS (cerebral, ocular, dental, auricular, skeletal) syndrome]] | |||
*[[Coffin-Lowry syndrome]] | |||
*[[Cohen syndrome]] | |||
*[[Cornelia de Lange syndrome]] | |||
*[[Craniomandibular dermatodysostosis]] | |||
*[[Cri du chat syndrome 5p−]] | |||
*[[De la Chapelle dysplasia]] | |||
*[[Diamond-Blackfan anemia]] | |||
*[[DiGeorge's syndrome]] | |||
*[[Dubowitz syndrome]] | |||
*[[Femoral hypoplasia - unusual facies syndrome]] | |||
*[[Fetal akinesia-hypokinesia sequence]] | |||
*[[Fetal aminopterin-like syndrome]] | |||
*[[Hurst's microtia-absent patellae-micrognathia syndrome]] | |||
*[[Juvenile chronic arthritis]] | |||
*[[Kyphomelic dysplasia]] | |||
*[[Lathosterolosis]] | |||
*[[Lethal congenital contracture syndrome]] | |||
*[[Lethal restrictive dermopathy]] | |||
*[[Loeys-Dietz syndrome]] | |||
*[[Lujan-Fryns syndrome]] | |||
*[[Marden-Walker syndrome]] | |||
*[[Marfan's syndrome]] | |||
*[[Micrognathia with peromelia]] | |||
*[[Miller-Dieker syndrome]] | |||
*[[Nager acrofacial dysostosis]] | |||
*[[Noonan's syndrome]] | |||
*[[Opitz-Frias syndrome]] | |||
*[[Orofaciodigital syndrome type 4]] | |||
*[[Otopalatodigital syndrome type 2]] | |||
*[[Pallister-Hall syndrome]] | |||
*[[Pierre Robin syndrome]] | |||
*[[Postaxial acrofacial dysostosis syndrome]] | |||
*[[Rothmund-Thomson syndrome]] | |||
*[[Schwartz-Jampel-Aberfeld syndrome]] | |||
*[[Scott craniodigital syndrome]] | |||
*[[Smith-Lemli-Opitz syndrome]] | |||
*[[Syphilis, congenital]] | |||
*[[Ter Haar syndrome]] | |||
*[[Toriello-Carey syndrome]] | |||
*[[Treacher Collins-Franceschetti syndrome]] | |||
*[[Trichorhinophalangeal syndrome type 1]] | |||
*[[Trichorhinophalangeal syndrome type 3]] | |||
*[[Turner's syndrome]] | |||
*[[Van Bogaert-Hozay syndrome]] | |||
*[[Wagner vitreoretinal degeneration syndrome]] | |||
*[[Weissenbacher-Zweymuller syndrome]] | |||
*[[Wolf-Hirschhorn syndrome]] | |||
*[[Yunis-Varon syndrome]] | |||
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-rays|X-Ray testing]]. | |||
==References== | |||
{{Reflist|2}} | |||
{{Oral pathology}} | {{Oral pathology}} | ||
<br> | <br> | ||
[[nl: Micrognathie]] | [[nl: Micrognathie]] | ||
Latest revision as of 23:42, 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]
|
WikiDoc Resources for Micrognathism |
|
Articles |
|---|
|
Most recent articles on Micrognathism Most cited articles on Micrognathism |
|
Media |
|
Powerpoint slides on Micrognathism |
|
Evidence Based Medicine |
|
Clinical Trials |
|
Ongoing Trials on Micrognathism at Clinical Trials.gov Trial results on Micrognathism Clinical Trials on Micrognathism at Google
|
|
Guidelines / Policies / Govt |
|
US National Guidelines Clearinghouse on Micrognathism NICE Guidance on Micrognathism
|
|
Books |
|
News |
|
Commentary |
|
Definitions |
|
Patient Resources / Community |
|
Patient resources on Micrognathism Discussion groups on Micrognathism Patient Handouts on Micrognathism Directions to Hospitals Treating Micrognathism Risk calculators and risk factors for Micrognathism
|
|
Healthcare Provider Resources |
|
Causes & Risk Factors for Micrognathism |
|
Continuing Medical Education (CME) |
|
International |
|
|
|
Business |
|
Experimental / Informatics |
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.