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[Clinical study of neurofibromatosis type 1].
- Source :
-
Revista de neurologia [Rev Neurol] 1998 Nov; Vol. 27 (159), pp. 792-5. - Publication Year :
- 1998
-
Abstract
- Introduction: Recklinghausen's disease is considered to be the autosomal dominant disorder with the highest rate of mutation after achondroplasia. It is a neuroectodermal disorder with considerable clinical effects.<br />Patients and Methods: We present a study of 14 patients seen for café-au-lait spots in the Clinical Genetics Department of the Hospital Infantil Sur. A detailed questionnaire and physical examination was done to obtain a clinical outline.<br />Conclusion: Suspicion of this condition, together with laboratory investigations led to the conclusion that the cases were neurofibromatosis.
- Subjects :
- Adolescent
Adult
Cafe-au-Lait Spots epidemiology
Cafe-au-Lait Spots etiology
Child
Child, Preschool
Cuba epidemiology
Diagnostic Imaging
Dwarfism epidemiology
Dwarfism etiology
Electroencephalography
Female
Humans
Infant
Intellectual Disability epidemiology
Intellectual Disability etiology
Magnetic Resonance Imaging
Male
Melanosis
Neurofibromatosis 1 epidemiology
Neurofibromatosis 1 pathology
Scoliosis epidemiology
Scoliosis etiology
Tomography, X-Ray Computed
Neurofibromatosis 1 diagnosis
Subjects
Details
- Language :
- Spanish; Castilian
- ISSN :
- 0210-0010
- Volume :
- 27
- Issue :
- 159
- Database :
- MEDLINE
- Journal :
- Revista de neurologia
- Publication Type :
- Academic Journal
- Accession number :
- 9859153