Abstract
The age of appearance and diagnostic value of the major defining features of von Recklinghausen neurofibromatosis (NF-1) have been studied in 168 cases from 73 families. In assessing children of an affected patient, those who have inherited the gene can be distinguished from their normal sibs on the basis of whether or not café au lait (CAL) spots are present by the age of five years. Lisch nodules appear before cutaneous neurofibromas and are a useful clinical aid in the assessment of unusual cases, those in whom the diagnosis is equivocal, and children with multiple CAL spots but no family history of NF-1. Sixty-nine of the families were identified through a population based study in south east Wales and the frequency of complications in 135 affected subjects from these families has been used to develop figures for genetic counselling. For these purposes, the complications of NF-1 can be usefully divided into four categories: intellectual handicap (33%) (moderate/severe retardation 3.2%, minimal retardation/learning difficulties 29.8%); complications developing in childhood and causing lifelong morbidity (8.5%); 'treatable' complications which can develop at any age (15.7%); and malignant or CNS tumours (4.4 to 5.2%).
MeSH Terms
Adolescent
Adult
Age Factors
Aged
Aged, 80 and over
Child
Child, Preschool
Female
Genetic Counseling
Humans
Infant
Intellectual Disability/etiology,genetics
Male
Middle Aged
Neurofibromatosis 1/complications,genetics
Peripheral Nervous System Neoplasms/etiology,genetics
Pigmentation Disorders/etiology,genetics
Rhabdomyosarcoma/etiology,genetics
Scoliosis/etiology,genetics
Skin Neoplasms/complications,genetics
Wales
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Huson S M
Institute of Medical Genetics, University of Wales College of Medicine, Heath Park, Cardiff.
Compston D A
Harper P S
References (23)
23 references, click to expand
-
Von Recklinghausen's disease: a clinicopathological study.
Ann Surg. 1972 Jan;175(1):86-104
PMID: 4621893
-
Clinical and genetic investigations into tuberous sclerosis and Recklinghausen's neurofibromatosis; contribution to elucidation of interrelationship and eugenics of the syndromes.
Acta Psychiatr Neurol Scand Suppl. 1951;71:1-239
PMID: 14877597
-
Pulsating enophthalmos and choroidal hamartomas: two rare stigmata of neurofibromatosis.
Br J Ophthalmol. 1977 Jul;61(7):483-8
PMID: 407919
-
Phaeochromocytomas in 72 patients: clinical and diagnostic features, treatment and long term results.
Br J Surg. 1979 Jul;66(7):456-65
PMID: 466037
-
Penetrance and variability in neurofibromatosis: a genetic study of 60 families.
Birth Defects Orig Artic Ser. 1979;15(5B):271-81
PMID: 118780
-
Von Recklinghausen neurofibromatosis. Incidence of iris hamartomata.
Ophthalmology. 1981 Apr;88(4):348-54
PMID: 6789269
-
Congenital pseudarthrosis of the tibia.
J Bone Joint Surg Br. 1981;63-B(3):367-75
PMID: 6790551
-
Malignancy in neurofibromatosis.
Adv Neurol. 1981;29:33-56
PMID: 6798842
-
Café-au-lait spots in schoolchildren.
Arch Dis Child. 1982 Aug;57(8):631-2
PMID: 6810767
-
Brief clinical report: aqueductal stenosis leading to hydrocephalus--an unusual manifestation of neurofibromatosis.
Am J Med Genet. 1983 Mar;14(3):577-81
PMID: 6407319
-
von Recklinghausen neurofibromatosis. II. Incidence of optic gliomata.
Ophthalmology. 1984 Aug;91(8):929-35
PMID: 6436764
-
Gliomas in neurofibromatosis: a series of 89 cases with evidence for enhanced malignancy in associated cerebellar astrocytomas.
Pathol Annu. 1985;20 Pt 1:331-58
PMID: 3921930
-
Prevalence of congenital-nevus-like nevi, nevi spili, and café au lait spots.
Arch Dermatol. 1985 Jun;121(6):766-9
PMID: 4004301
-
Iris (Lisch) nodules in neurofibromatosis.
Clin Genet. 1986 Jan;29(1):51-5
PMID: 3081287
-
Linkage analysis of peripheral neurofibromatosis (Von Recklinghausen disease) and chromosome 19 markers linked to myotonic dystrophy.
J Med Genet. 1986 Feb;23(1):55-7
PMID: 3081725
-
Iris hamartomata as diagnostic criterion in neurofibromatosis.
Neuropediatrics. 1986 Nov;17(4):183-5
PMID: 3100979
-
Ophthalmic manifestations of neurofibromatosis.
Br J Ophthalmol. 1987 Mar;71(3):235-8
PMID: 3103673
-
Duodenal carcinoid tumours, phaeochromocytoma and neurofibromatosis: islet cell tumour, phaeochromocytoma and the von Hippel-Lindau complex: two distinctive neuroendocrine syndromes.
Q J Med. 1987 Sep;64(245):769-82
PMID: 2897130
-
Multipoint linkage analysis in neurofibromatosis type I: an international collaboration.
Am J Hum Genet. 1989 Jan;44(1):6-12
PMID: 2491784
-
Von Recklinghausen neurofibromatosis. A clinical and population study in south-east Wales.
Brain. 1988 Dec;111 ( Pt 6):1355-81
PMID: 3145091
-
A genetic study of von Recklinghausen neurofibromatosis in south east Wales. I. Prevalence, fitness, mutation rate, and effect of parental transmission on severity.
J Med Genet. 1989 Nov;26(11):704-11
PMID: 2511318
-
Neurofibromatosis in children with soft tissue sarcoma.
Pediatr Hematol Oncol. 1988;5(1):7-16
PMID: 3155239
-
Neurofibromatous scoliosis. Natural history and results of treatment in thirty-seven cases.
J Bone Joint Surg Am. 1976 Jul;58(5):695-702
PMID: 819447