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 23:09, 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 , Pierre Robin syndrome, 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

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 ==Causes==
-,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
+*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 [[DiGeorge's Syndrome]], [[Pierre Robin syndrome]], [[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]].
+Its causes also include , [[Pierre Robin syndrome]], [[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==