Micrognathism: Difference between revisions
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{{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}} | ||
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==Causes== | ==Causes== | ||
*49,XXXXX | *[[49,XXXXX syndrome]] | ||
*Atkin-Flaitz-Patil | *[[Atkin-Flaitz-Patil syndrome]] | ||
*Bowen-Conradi | *[[Bowen-Conradi syndrome]] | ||
*Camptomelic | *[[Camptomelic dysplasia]] | ||
*Cardiofaciocutaneous | *[[Cardiofaciocutaneous syndrome]] | ||
*Carey-Fineman-Ziter | *[[Carey-Fineman-Ziter syndrome]] | ||
*Catel-Manzke | *[[Catel-Manzke syndrome]] | ||
*Cerebrocostomandibular | *[[Cerebrocostomandibular syndrome]] | ||
*Cerebrohepatorenal | *[[Cerebrohepatorenal syndrome]] | ||
*CHARGE | *[[CHARGE syndrome]] | ||
*Chromosome | *[[Chromosome 18 trisomy syndrome]] | ||
*Chromosome | *[[Chromosome 8 recombinant syndrome]] | ||
*Chromosome | *[[Chromosome 8 trisomy syndrome]] | ||
*CODAS | *[[CODAS (cerebral, ocular, dental, auricular, skeletal) syndrome]] | ||
*Coffin-Lowry | *[[Coffin-Lowry syndrome]] | ||
*Cohen | *[[Cohen syndrome]] | ||
*Cornelia | *[[Cornelia de Lange syndrome]] | ||
*Craniomandibular | *[[Craniomandibular dermatodysostosis]] | ||
*Cri | *[[Cri du chat syndrome 5p−]] | ||
*De | *[[De la Chapelle dysplasia]] | ||
*Diamond-Blackfan | *[[Diamond-Blackfan anemia]] | ||
*DiGeorge's | *[[DiGeorge's syndrome]] | ||
*Dubowitz | *[[Dubowitz syndrome]] | ||
*Femoral hypoplasia - unusual | *[[Femoral hypoplasia - unusual facies syndrome]] | ||
*Fetal | *[[Fetal akinesia-hypokinesia sequence]] | ||
*Fetal | *[[Fetal aminopterin-like syndrome]] | ||
*Hurst's | *[[Hurst's microtia-absent patellae-micrognathia syndrome]] | ||
*Juvenile | *[[Juvenile chronic arthritis]] | ||
*Kyphomelic | *[[Kyphomelic dysplasia]] | ||
*Lathosterolosis | *[[Lathosterolosis]] | ||
*Lethal | *[[Lethal congenital contracture syndrome]] | ||
*Lethal | *[[Lethal restrictive dermopathy]] | ||
*Loeys-Dietz | *[[Loeys-Dietz syndrome]] | ||
*Lujan-Fryns | *[[Lujan-Fryns syndrome]] | ||
*Marden-Walker | *[[Marden-Walker syndrome]] | ||
*Marfan's | *[[Marfan's syndrome]] | ||
*Micrognathia | *[[Micrognathia with peromelia]] | ||
*Miller-Dieker | *[[Miller-Dieker syndrome]] | ||
*Nager | *[[Nager acrofacial dysostosis]] | ||
*Noonan's | *[[Noonan's syndrome]] | ||
*Opitz-Frias | *[[Opitz-Frias syndrome]] | ||
*Orofaciodigital | *[[Orofaciodigital syndrome type 4]] | ||
*Otopalatodigital | *[[Otopalatodigital syndrome type 2]] | ||
*Pallister-Hall | *[[Pallister-Hall syndrome]] | ||
*Pierre | *[[Pierre Robin syndrome]] | ||
*Postaxial | *[[Postaxial acrofacial dysostosis syndrome]] | ||
*Rothmund-Thomson | *[[Rothmund-Thomson syndrome]] | ||
*Schwartz-Jampel-Aberfeld | *[[Schwartz-Jampel-Aberfeld syndrome]] | ||
*Scott | *[[Scott craniodigital syndrome]] | ||
*Smith-Lemli-Opitz | *[[Smith-Lemli-Opitz syndrome]] | ||
*Syphilis, | *[[Syphilis, congenital]] | ||
*Ter | *[[Ter Haar syndrome]] | ||
*Toriello-Carey | *[[Toriello-Carey syndrome]] | ||
*Treacher | *[[Treacher Collins-Franceschetti syndrome]] | ||
*Trichorhinophalangeal | *[[Trichorhinophalangeal syndrome type 1]] | ||
*Trichorhinophalangeal | *[[Trichorhinophalangeal syndrome type 3]] | ||
*Turner's | *[[Turner's syndrome]] | ||
*Van | *[[Van Bogaert-Hozay syndrome]] | ||
*Wagner | *[[Wagner vitreoretinal degeneration syndrome]] | ||
*Weissenbacher-Zweymuller | *[[Weissenbacher-Zweymuller syndrome]] | ||
*Wolf-Hirschhorn | *[[Wolf-Hirschhorn syndrome]] | ||
*Yunis-Varon | *[[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== | ||
===Skull X ray=== | ===Skull X ray=== | ||
It can be detected by dental or skull [[X-rays|X-Ray testing]]. | It can be detected by dental or skull [[X-rays|X-Ray testing]]. | ||
==References== | ==References== |
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 |
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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
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Guidelines / Policies / Govt |
US National Guidelines Clearinghouse on Micrognathism NICE Guidance on Micrognathism
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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
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Healthcare Provider Resources |
Causes & Risk Factors for Micrognathism |
Continuing Medical Education (CME) |
International |
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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.