Cantú syndrome: A new case and evolution of clinical conditions during first 2‐year follow‐up
Cantú syndrome: A new case and evolution of clinical conditions during first 2‐year follow‐up
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Publisher
England: John Wiley & Sons, Inc
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Language
English
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Publisher
England: John Wiley & Sons, Inc
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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 appearance and cardiac involvement, with a de novo he...
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Full title
Cantú syndrome: A new case and evolution of clinical conditions during first 2‐year follow‐up
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TN_cdi_doaj_primary_oai_doaj_org_article_7c9ba5a760a44343a65d0f6f8ac4d05d
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_7c9ba5a760a44343a65d0f6f8ac4d05d
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ISSN
2050-0904
E-ISSN
2050-0904
DOI
10.1002/ccr3.6928
