Cantú syndrome: A new case and evolution of clinical conditions during first 2‐year follow‐up

Cantú syndrome, or hypertrichotic osteochondrodysplasia, is a rare autosomal dominant disease characterized by congenital hypertrichosis, characteristic dysmorphisms, skeletal abnormalities and cardiomegaly. We report on a 7‐year‐old girl with congenital generalized hypertrichosis, coarse facial app...

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Detalles Bibliográficos
Autores principales: Mattiucci, Alessandra, Girolomoni, Giampiero, Cassina, Matteo, Zoller, Thomas, Antoniazzi, Franco, Schena, Donatella
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9979969/
https://www.ncbi.nlm.nih.gov/pubmed/36873080
http://dx.doi.org/10.1002/ccr3.6928

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9979969/
https://www.ncbi.nlm.nih.gov/pubmed/36873080
http://dx.doi.org/10.1002/ccr3.6928

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