ISSN:
1432-1459
Keywords:
Familial glioma
;
Phakomatosis
;
Familial cancer syndrome
;
“Two-hit-model”
;
Cancer genetics
Source:
Springer Online Journal Archives 1860-2000
Topics:
Medicine
Notes:
Summary The family pedigree across eight generations is presented with an association of osteochondrodysplasia, other skeletal abnormalities, familial glial tumours in a father and his son, colonic and other adenomatous disease, and pigment changes. This family cluster of diseases is considered to be a dysontogenetic process with blastomatous features and grouped within the phakomastoses. A review of the literature indicates that some “familial gliomas” show additional malformations, thus resembling phakomatoses. Others are found to be members within a “familial cancer syndrome”. A trait of “hereditary glioma” apart from these syndromes is difficult to identify, especially if only sibships are considered which are likely to share common environmental factors.
Type of Medium:
Electronic Resource
URL:
http://dx.doi.org/10.1007/BF00618254
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