Abstract
We report on a 16-month-old girl with multiple swellings on her skull due to massive osteolysis, growth retardation, facial anomalies, and wrinkly skin with mosaic hypopigmentation. She also had severe hypercalcemia, which gradually returned to normal levels. The condition likely represents Gorham syndrome with systemic manifestations.
| Original language | English |
|---|---|
| Pages (from-to) | 759-763 |
| Number of pages | 5 |
| Journal | American Journal of Medical Genetics, Part A |
| Volume | 152 |
| Issue number | 3 |
| DOIs | |
| Publication status | Published - 03-2010 |
All Science Journal Classification (ASJC) codes
- Genetics
- Genetics(clinical)
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