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Micrognathism

Known as: Micrognathia, Mandibular, MICROGNATHIA, Mandible small 
A congenital abnormality of the jaws (particularly the mandible) in which they are unusually small. This condition is not always pathological and may… 
National Institutes of Health

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Related topics

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ARTERIAL TORTUOSITY SYNDROMEAcrootoocular SyndromeAtelosteogenesis Type 3Atelosteogenesis type 2

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Schweitzer Kemink Graham syndrome

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
1991
1991
A malformed child with a recombinant chromosome 7, rec(7) dup p, derived from a maternal pericentric inversion inv(7)(p15q36).
We report a child with facial dysmorphic features, hypoplasia of the external genitalia, intestinal malrotation, congenital… 
1987
1987
Three new genera and five new species of misophrioid copepods (Crustacea) from anchialine caves on Indo‐West Pacific and North Atlantic Islands
Misophrioid copepods are described from anchialine caves on Palau, Western Caroline Islands and on Lanzarote, Canary Islands. A… 
1977
1977
Hypersomnolence and intermittent upper airway obstruction. Occurrence caused by micrognathia.
A patient with hypersomnolence, micrognathia, and respiratory insufficiency had been treated eight years for narcolepsy. Sleep… 
Highly Cited
1975
Highly Cited
1975
Chromosome 3 duplication q21 leads to qter deletion p25 leads to pter syndrome in children of carriers of a pericentric inversion inv(3) (p25q21).
Close phenotypic similarity between two cases carrying a rec(3) dup q,inv(3) (p25q21), 12 additional infants from the same inv (3… 
Review
1975
Review
1975
Trisomy 22. Two new cases and delineation of the phenotype.
Two unrelated children, not affected with Down's syndrome, with strikingly similar phenotypes and an extra G-like chromosome are… 
1974
1974
21 Monosomy in a retarded female infant
A 20-month-old female infant with complete monosomy 21 is described. She has marked mental and physical retardation… 
1972
1972
Mosaicism with translocation: autoradiographic and fluorescent studies of an inherited reciprocal translocation t(2q+;14q-).
The propositus was born on 12 July 1970 after a fullterm gestation. The father was 26. The mother was 21 years old; she had… 
Highly Cited
1971
Highly Cited
1971
The 4p- syndrome. A clinically recognizable chromosomal deletion syndrome.
Partial deletion of the short arm of chromosome 4 results in a clinically recognizable and distinct syndrome. Common features… 
1964
1964
MANDIBULAR GROWTH AND DENTAL OCCLUSION IN JUVENILE RHEUMATOID ARTHRITIS.
Summary and ConclusionsThe effect of juvenile rheumatoid arthritis on mandibular growth and the dental occlusion in nineteen… 
1950
1950
Further report on the treatment of micrognathia with obstruction by a plastic procedure; results based on reports from 21 cities; 1948-1949.
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