Relationship between café-au-lait spots as the only symptom and peripheral neurofibromatosis (NF1): A follow-up study
- 1 June 1993
- journal article
- Published by Springer Nature in European Journal of Pediatrics
- Vol. 152 (6) , 500-504
- https://doi.org/10.1007/bf01955059
Abstract
We re-examined 21 children with the possible diagnosis of peripheral neurofibromatosis (NF1) based on the presence of café-au-lait (CAL) spots as the single clinical finding. We evaluated whether "typical" or "atypical" appearance of the spots was important for the final diagnosis and whether the co-existence of other non-specific signs (e.g. pectus excavatum) were of any significance for the final diagnosis. In 8/14 (57.1%) cases with "typical" CAL spots, the diagnosis of NF1 was finally established on the basis of other criteria. For the other 6 patients the diagnosis is not yet definitive but highly probable on the basis of the presence of macrocephaly, pectus excavatum and/or MRI findings. Only one patient among five with "atypical" CAL spots possibly has NF1.Keywords
This publication has 13 references indexed in Scilit:
- cDNA cloning of the type 1 neurofibromatosis gene: Complete sequence of the NF1 gene productGenomics, 1991
- Type 1 Neurofibromatosis Gene: Identification of a Large Transcript Disrupted in Three NF1 PatientsScience, 1990
- A major segment of the neurofibromatosis type 1 gene: cDNA sequence, genomic structure, and point mutationsPublished by Elsevier ,1990
- The significance of MRI abnormalities in children with neurofibromatosisNeurology, 1989
- NeurofibromatosisArchives of Neurology, 1988
- NeurofibromatosisPublished by Elsevier ,1987
- Macromelanosomes in the Early Diagnosis of NeurofibromatosisThe American Journal of Dermatopathology, 1986
- Melanin Macroglobules As a Cellular Marker of Neurofibromatosis: A Quantitative StudyJournal of Investigative Dermatology, 1985
- Von Recklinghausen NeurofibromatosisNew England Journal of Medicine, 1981
- von Recklinghausen NeurofibromatosisOphthalmology, 1981