Cantu syndrome and hypopituitarism: implications for endocrine monitoring

SUMMARY: Cantu syndrome, or hypertrichotic osteochondrodysplasia, is a rare, autosomal dominant genetically heterogeneous disorder. It is characterized by hypertrichosis, cardiac and skeletal anomalies and distinctive coarse facial features. We report a case where slowed growth velocity at 13 years...

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Detalles Bibliográficos
Autores principales: Theis, Nicholas J, Calvert, Toby, McIntyre, Peter, Robertson, Stephen P, Wheeler, Benjamin J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bioscientifica Ltd 2019
Materias:
Unique/Unexpected Symptoms or Presentations of a Disease
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6865860/
https://www.ncbi.nlm.nih.gov/pubmed/31743099
http://dx.doi.org/10.1530/EDM-19-0103

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6865860/
https://www.ncbi.nlm.nih.gov/pubmed/31743099
http://dx.doi.org/10.1530/EDM-19-0103

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