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 |
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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 |