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Axenfeld–Rieger syndrome

Axenfeld–Rieger syndrome Axenfeld–Rieger syndrome is an inherited developmental disorder linked in this packet to PITX2 mutations.

Axenfeld–Rieger syndrome is an inherited developmental disorder linked in this packet to PITX2 mutations. It involves abnormal development of the front part of the eye along with underdeveloped teeth, distinctive craniofacial differences, and umbilical abnormalities.

Sources

Drafting source: Liu Yi; Semina Elena V.. pitx2 Deficiency Results in Abnormal Ocular and Craniofacial Development in Zebrafish. 2012; DOI 10.1371/journal.pone.0030896; article XML SHA-256 426e12f0c93fa51ace9bfdcfee7c4c42e210dadb986a8eb942fdc162a8ff5916. “pitx2 Deficiency Results in Abnormal Ocular and Craniofacial Development in Zebrafish” (10.1371/journal.pone.0030896).
CC-BY-4.0 · Definition uses new wording; original source retains its stated licence. · Source snapshot SHA-256: 426e12f0c93fa51ace9bfdcfee7c4c42e210dadb986a8eb942fdc162a8ff5916

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PsychTerms (psychterms.org), CC BY 4.0, version 1. “Axenfeld–Rieger syndrome.” Development preview.

Version 1 · SHA-256: 4b6e3141654a658a451040cd780044477ba549bc38089031508d53124c7dd774

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Axenfeld–Rieger syndrome

See also

Sources

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