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Because pseudoacromegaly conditions are rare and heterogeneous, often with overlapping clinical features, the underlying diagnosis may be challenging to establish. As many of these have a genetic origin, such as pachydermoperiostosis, Sotos syndrome, Weaver syndrome, or Cant\u00fa syndrome, collaboration is key with clinical geneticists in the diagnosis of these patients. Although rare, awareness of these uncommon conditions and their characteristic features will help their timely recognition.<\/jats:p>","DOI":"10.1210\/clinem\/dgab789","type":"journal-article","created":{"date-parts":[[2021,11,18]],"date-time":"2021-11-18T12:23:19Z","timestamp":1637238199000},"page":"1767-1788","source":"Crossref","is-referenced-by-count":14,"title":["Approach to the Patient With Pseudoacromegaly"],"prefix":"10.1210","volume":"107","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-4959-5725","authenticated-orcid":false,"given":"Pedro","family":"Marques","sequence":"first","affiliation":[{"name":"Centre for Endocrinology, William Harvey Research Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, EC1M 6BQ London, UK"},{"name":"Endocrinology Department, Hospital de Santa Maria, Centro Hospitalar Universit\u00e1rio de Lisboa Norte, Lisboa, Portugal"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-4101-9432","authenticated-orcid":false,"given":"M\u00e1rta","family":"Korbonits","sequence":"additional","affiliation":[{"name":"Centre for Endocrinology, William Harvey Research Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, EC1M 6BQ London, UK"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"80","published-online":{"date-parts":[[2021,11,18]]},"reference":[{"key":"2022051722345117500_CIT0001","doi-asserted-by":"crossref","first-page":"113","DOI":"10.1016\/j.yfrne.2018.11.001","article-title":"Pseudoacromegaly","volume":"52","author":"Marques","year":"2019","journal-title":"Front Neuroendocrinol."},{"issue":"3","key":"2022051722345117500_CIT0002","doi-asserted-by":"crossref","first-page":"677","DOI":"10.1007\/s12020-017-1497-9","article-title":"Cant\u00fa syndrome with coexisting familial pituitary 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