Abstract
A child with Noonan syndrome and multiple cafe au lait spots, compatible in size and number with von Recklinghausen's neurofibromatosis, is presented. These featurs may represent a distinct genetic entity rather than the coincidence of two diseases.
| Original language | English |
|---|---|
| Pages (from-to) | 196-198 |
| Number of pages | 3 |
| Journal | Archives of Disease in Childhood |
| Volume | 62 |
| Issue number | 2 |
| DOIs | |
| State | Published - 1987 |
| Externally published | Yes |