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Condition

First Arch Syndrome

Congenital Malformations and Chromosomal Abnormalities

First arch syndromes are congenital defects caused by a failure of neural crest cells to migrate into the first pharyngeal arch during embryonic development. They can produce facial anomalies, and examples of first arch syndromes include Treacher Collins syndrome and Pierre Robin syndrome.

Facts
Classification
Body System
Nervous System 1
ICD-10 Chapter
XVII: Congenital Malformations, Deformations and Chromosomal Abnormalities 2
Communicable or Non-communicable
Non-Communicable 3
Transmission Route
Non-Transmissible 4
Sources
1. Wikidata: First Arch Syndrome
WikidataWikidata P279 (body-system: nervous)
Quote, Wikidata P279 (body-system: nervous)
Subclass of: neurocristopathy
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2. Wikipedia: ICD-10
WikipediaList of chapters, Chapter XVII
Quote, List of chapters, Chapter XVII
Congenital malformations, deformations and chromosomal abnormalities
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3. Wikipedia: Non-communicable disease
WikipediaInherited/genetic diseases section
Quote, Inherited/genetic diseases section
Genetic disorders are caused by errors in genetic information that produce diseases in the affected people.
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4. Wikipedia: First arch syndrome
WikipediaLead section, transmission-route statement
Quote, Lead section, transmission-route statement
First arch syndromes are congenital defects caused by a failure of neural crest cells to migrate into the first pharyngeal arch.
View the Source
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