Cantu syndrome and hypopituitarism: implications for endocrine monitoring
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 led to id...
| Main Authors: | , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Bioscientifica
2019-11-01
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| Series: | Endocrinology, Diabetes & Metabolism Case Reports |
| Online Access: | https://doi.org/10.1530/EDM-19-0103 |