Achalasia microcephaly

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Revision as of 23:17, 5 November 2022 by Oldver>Mehrdad (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).")

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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).

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