| phakomatosis | A generic term for a group of hereditary diseases characterised by hamartomas involving multiple tissues; e.g., von Hippel-Lindau's disease, neurofibromatosis, Sturge-Weber syndrome, tuberous sclerosis. Synonym: phakomatosis. Origin: Van der Hoeve's coinage fr. G. Phakos, mother-spot (05 Mar 2000) |
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| phakomatosis |
pl. phakomato´ses [phakoma + -osis] any of a group of congenital and hereditary developmental anomalies having in common selective involvement of the tissues of ectodermal origin (i.e., central nervous system, eye, and skin) and the development of disseminated glial hamartomas (phakomas) in these tissues. The major syndromes in the group are neurofibromatosis, tuberous sclerosis, Sturge-Weber syndrome, von Hippel-Lindau disease, and ataxia-telangiectasia. Called also neurocutaneous syndrome. Written also phacomatosis.
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