Micrognathism: Difference between revisions

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List of terms related to Micrognathism

	Micrognathism;
ICD-10	K07.0
ICD-9	524.04
DiseasesDB	22641
MedlinePlus	003306
MeSH	D008844

VisualWikitext

Revision as of 23:13, 29 July 2012

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

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

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-Ray testing.

References

Template:Oral pathology

nl: Micrognathie

Template:WH Template:WikiDoc Sources

@@ Line 1: / Line 1: @@
 {{Infobox_Disease |
-  Name           = Micrognathism |
+Name      = Micrognathism |
-  Image          = |
+ Image     = |
-  Caption        = |
+ Caption    = |
-   DiseasesDB     = 22641 |
+ DiseasesDB   = 22641 |
-  ICD10          = {{ICD10|K|07|0|k|00}} |
+ ICD10     = {{ICD10|K|07|0|k|00}} |
-  ICD9           = {{ICD9|524.04}} |
+ ICD9      = {{ICD9|524.04}} |
-  ICDO           = |
+ ICDO      = |
-  OMIM           = |
+ OMIM      = |
-  MedlinePlus    = 003306 |
+ MedlinePlus  = 003306 |
-  eMedicineSubj  = |
+ eMedicineSubj = |
-  eMedicineTopic = |
+ eMedicineTopic = |
-  MeshID         = D008844 |
+ MeshID     = D008844 |
 }}
 {{CMG}}
@@ Line 26: / Line 26: @@
 ==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 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]]
-*[[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 , , [[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]].