Achalasia microcephaly: Revision history

Jump to navigation Jump to search

Diff selection: Mark the radio buttons of the revisions to compare and hit enter or the button at the bottom.
Legend: (cur) = difference with latest revision, (prev) = difference with preceding revision, m = minor edit.

23 March 2023

6 November 2022

  • curprev 00:1700:17, 6 November 2022Oldver>Mehrdad 248 bytes +248 Created page with "* An extremely rare '''genetic syndrome''' characterized by the association of microcephaly, intellectual deficit and achalasia (with symptoms of coughing, dysphagia, vomiting, failure to thrive and aspiration appearing in infancy/early-childhood)."